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ORCIDBioinformatics, Volume 28
Volume 28, Number 1, January 2012
- Yang Chen, Jin Gu
, Dan Li, Shao Li:
Time-course network analysis reveals TNF-α can promote G1/S transition of cell cycle in vascular endothelial cells. 1-4
- Minzhu Xie, Jing Li, Tao Jiang:
Detecting genome-wide epistases based on the clustering of relatively frequent items. 5-12
- Guohui Yao, Liang Ye, Hongyu Gao, Patrick Minx, Wesley C. Warren, George M. Weinstock:
Graph accordance of next-generation sequence assemblies. 13-16 - David Langenberger, Sachin Pundhir, Claus Thorn Ekstrøm, Peter F. Stadler, Steve Hoffmann, Jan Gorodkin:
deepBlockAlign: a tool for aligning RNA-seq profiles of read block patterns. 17-24 - Natsuhiro Ichinose, Tetsushi Yada, Osamu Gotoh:
Large-scale motif discovery using DNA Gray code and equiprobable oligomers. 25-31 - Dapeng Li, Tonghua Li, Peisheng Cong, Wenwei Xiong, Jiangming Sun:
A novel structural position-specific scoring matrix for the prediction of protein secondary structures. 32-39 - Arief Gusnanto, Henry M. Wood, Yudi Pawitan, Pamela Rabbitts, Stefano Berri:
Correcting for cancer genome size and tumour cell content enables better estimation of copy number alterations from next-generation sequence data. 40-47
- Ryan M. Ames, Daniel Money, Vikramsinh P. Ghatge, Simon Whelan, Simon C. Lovell:
Determining the evolutionary history of gene families. 48-55
- Gabriel Cuéllar-Partida, Fabian A. Buske, Robert C. McLeay, Tom Whitington, William Stafford Noble, Timothy L. Bailey:
Epigenetic priors for identifying active transcription factor binding sites. 56-62 - Ming Hu, Yu Zhu, Jeremy M. G. Taylor, Jun S. Liu, Zhaohui S. Qin:
Using Poisson mixed-effects model to quantify transcript-level gene expression in RNA-Seq. 63-68
- Stefan Maetschke, Martin Simonsen, Melissa J. Davis, Mark A. Ragan:
Gene Ontology-driven inference of protein-protein interactions using inducers. 69-75 - Nicola Soranzo, Fahimeh Ramezani, Giovanni Iacono, Claudio Altafini:
Decompositions of large-scale biological systems based on dynamical properties. 76-83 - Emmanuelle Becker, Benoît Robisson, Charles E. Chapple, Alain Guénoche, Marie-Christine Brun:
Multifunctional proteins revealed by overlapping clustering in protein interaction network. 84-90 - Muhammad Tahir, Asifullah Khan, Abdul Majid:
Protein subcellular localization of fluorescence imagery using spatial and transform domain features. 91-97 - Xiujun Zhang, Xing-Ming Zhao, Kun He, Le Lu, Yongwei Cao, Jingdong Liu, Jin-Kao Hao, Zhi-Ping Liu, Luonan Chen:
Inferring gene regulatory networks from gene expression data by path consistency algorithm based on conditional mutual information. 98-104 - Edward Y. Chen, Huilei Xu, Simon Gordonov, Maribel P. Lim, Matthew H. Perkins, Avi Ma'ayan:
Expression2Kinases: mRNA profiling linked to multiple upstream regulatory layers. 105-111
- Daniel J. Stekhoven, Peter Bühlmann:
MissForest - non-parametric missing value imputation for mixed-type data. 112-118
- Xavier Rafael Palou, Michael P. Schroeder, Núria López-Bigas:
SVGMap: configurable image browser for experimental data. 119-120 - Kun Liang, Sündüz Keles:
Detecting differential binding of transcription factors with ChIP-seq. 121-122 - Francesco Vezzi, Cristian Del Fabbro, Alexandru I. Tomescu, Alberto Policriti:
rNA: a fast and accurate short reads numerical aligner. 123-124
- Yongan Zhao, Haixu Tang, Yuzhen Ye:
RAPSearch2: a fast and memory-efficient protein similarity search tool for next-generation sequencing data. 125-126 - Manal Kalkatawi, Farania Rangkuti, Michael Schramm, Boris R. Jankovic, Allan Kamau, Rajesh Chowdhary, John A. C. Archer, Vladimir B. Bajic:
Dragon PolyA Spotter: predictor of poly(A) motifs within human genomic DNA sequences. 127-129 - Marc Torrent, Paolo Di Tommaso, David Pulido, Victòria M. Nogués, Cédric Notredame, Ester Boix, David Andreu:
AMPA: an automated web server for prediction of protein antimicrobial regions. 130-131 - Mattia C. F. Prosperi, Marco Salemi:
QuRe: software for viral quasispecies reconstruction from next-generation sequencing data. 132-133
- Céline Bellenguez, Amy Strange, Colin Freeman, Peter Donnelly, Chris C. A. Spencer:
A robust clustering algorithm for identifying problematic samples in genome-wide association studies. 134-135
- Brian Pratt, J. Jeffry Howbert, Natalie I. Tasman, Erik J. Nilsson:
MR-Tandem: parallel X!Tandem using Hadoop MapReduce on Amazon Web Services. 136-137 - Walter Georgescu, John P. Wikswo, Vito Quaranta:
CellAnimation: an open source MATLAB framework for microscopy assays. 138-139
- Stephanie A. Canny, Yasel Cruz, Mark R. Southern, Patrick R. Griffin:
PubChem promiscuity: a web resource for gathering compound promiscuity data from PubChem. 140-141
- Erik Dassi, A. Malossini, Angela Re, Tommaso Mazza, Toma Tebaldi, Luigi Caputi, Alessandro Quattrone:
AURA: Atlas of UTR Regulatory Activity. 142-144
- Xiang Wan, Can Yang, Weichuan Yu:
Comments on 'An empirical comparison of several recent epistatic interaction detection methods'. 145-146
- Yue Wang, Guimei Liu, Mengling Feng, Limsoon Wong:
Response: an empirical comparison of several recent epistatic interaction detection methods. 147-148
- Marie Brown, David C. Wedge, Royston Goodacre, Douglas B. Kell, Philip N. Baker, Louise C. Kenny, Mamas A. Mamas, Ludwig Neyses, Warwick B. Dunn:
Automated workflows for accurate mass-based putative metabolite identification in LC/MS-derived metabolomic datasets. 149 - Farhad Hormozdiari, Faraz Hach, Süleyman Cenk Sahinalp, Evan E. Eichler, Can Alkan:
Sensitive and fast mapping of di-base encoded reads. 150
Volume 28, Number 2, January 2012
- Gerard Wong, Christopher Leckie, Adam Kowalczyk:
FSR: feature set reduction for scalable and accurate multi-class cancer subtype classification based on copy number. 151-159 - David R. Riley, Samuel V. Angiuoli, Jonathan Crabtree, Julie C. Dunning Hotopp, Hervé Tettelin:
Using Sybil for interactive comparative genomics of microbes on the web. 160-166
- Jiarui Ding, Ali Bashashati, Andrew Roth, Arusha Oloumi, Kane Tse, Thomas Zeng, Gholamreza Haffari, Martin Hirst, Marco A. Marra, Anne Condon, Sam Aparicio, Sohrab P. Shah:
Feature-based classifiers for somatic mutation detection in tumour-normal paired sequencing data. 167-175 - Yi-Fei Huang, Geoffrey Brian Golding:
Inferring sequence regions under functional divergence in duplicate genes. 176-183 - David T. Jones, Daniel W. A. Buchan, Domenico Cozzetto, Massimiliano Pontil:
PSICOV: precise structural contact prediction using sparse inverse covariance estimation on large multiple sequence alignments. 184-190
- Benjamin Albrecht, Céline Scornavacca, Alberto Cenci, Daniel H. Huson:
Fast computation of minimum hybridization networks. 191-197
- Anna Philips, Kaja Milanowska, Grzegorz Lach, Michal J. Boniecki, Kristian Rother, Janusz M. Bujnicki:
MetalionRNA: computational predictor of metal-binding sites in RNA structures. 198-205
- Mark Maienschein-Cline, Jie Zhou, Kevin P. White, Roger Sciammas, Aaron R. Dinner:
Discovering transcription factor regulatory targets using gene expression and binding data. 206-213 - Geert Geeven, Ronald E. van Kesteren, August B. Smit, Mathisca C. M. de Gunst:
Identification of context-specific gene regulatory networks with GEMULA - gene expression modeling using LAsso. 214-221 - Bettina Grün, Theresa Scharl, Friedrich Leisch:
Modelling time course gene expression data with finite mixtures of linear additive models. 222-228
- Hua Wang, Feiping Nie, Heng Huang, Sungeun Kim, Kwangsik Nho, Shannon L. Risacher, Andrew J. Saykin, Li Shen:
Identifying quantitative trait loci via group-sparse multitask regression and feature selection: an imaging genetics study of the ADNI cohort. 229-237
- Jose L. Rubio-Guivernau, Vasily Gurchenkov, Miguel A. Luengo-Oroz, Louise Duloquin, Paul Bourgine, Andrés Santos, Nadine Peyriéras, María J. Ledesma-Carbayo:
Wavelet-based image fusion in multi-view three-dimensional microscopy. 238-245
- José Caldas, Nils Gehlenborg, Eeva Kettunen, Ali Faisal, Mikko Rönty, Andrew G. Nicholson, Sakari Knuutila, Alvis Brazma, Samuel Kaski:
Data-driven information retrieval in heterogeneous collections of transcriptomics data links SIM2s to malignant pleural mesothelioma. 246-253 - Nathan Harmston, Wendy Filsell, Michael P. H. Stumpf:
Which species is it? Species-driven gene name disambiguation using random walks over a mixture of adjacency matrices. 254-260 - Jean-Philippe Carralot, Arnaud Ogier, Annette Boese, Auguste Genovesio, Priscille Brodin, Peter Sommer, Thierry Dorval:
A novel specific edge effect correction method for RNA interference screenings. 261-268
- Fidel Ramírez, Glenn Lawyer, Mario Albrecht:
Novel search method for the discovery of functional relationships. 269-276
- Yan W. Asmann, Sumit Middha, Asif Hossain, Saurabh Baheti, Ying Li, High-Seng Chai, Zhifu Sun, Patrick H. Duffy, Ahmed A. Hadad, Asha A. Nair, Xiaoyu Liu, Yuji Zhang, Eric W. Klee, Krishna R. Kalari, Jean-Pierre A. Kocher:
TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data. 277-278 - Pablo Librado, Filipe G. Vieira, Julio Rozas:
BadiRate: estimating family turnover rates by likelihood-based methods. 279-281 - Aristotelis Tsirigos, Niina Haiminen, Erhan Bilal, Filippo Utro:
GenomicTools: a computational platform for developing high-throughput analytics in genomics. 282-283
- R. W. W. Brouwer, M. C. G. N. van den Hout, Frank G. Grosveld, Wilfred F. J. van IJcken:
NARWHAL, a primary analysis pipeline for NGS data. 284-285
- Chi-Ho Ngan, David R. Hall, Brandon S. Zerbe, Laurie E. Grove, Dima Kozakov, Sandor Vajda:
FTSite: high accuracy detection of ligand binding sites on unbound protein structures. 286-287
- Laurent Gatto, Kathryn S. Lilley:
MSnbase-an R/Bioconductor package for isobaric tagged mass spectrometry data visualization, processing and quantitation. 288-289
- Christopher W. Whelan, M. Kemal Sönmez:
Computing graphlet signatures of network nodes and motifs in Cytoscape with GraphletCounter. 290-291 - Dominique F. Chu, Nicolae Radu Zabet, Tobias von der Haar:
A novel and versatile computational tool to model translation. 292-293 - Lu Zhang, Shengchang Gu, Yuan Liu, Bingqiang Wang, Francisco Azuaje:
Gene set analysis in the cloud. 294-295
- Nigel F. Reuel, Peter Bojo, Jingqing Zhang, Ardemis A. Boghossian, Jin-Ho Ahn, Jong-Ho Kim, Michael S. Strano:
NoRSE: noise reduction and state evaluator for high-frequency single event traces. 296-297 - Heidi E. L. Lischer, Laurent Excoffier:
PGDSpider: an automated data conversion tool for connecting population genetics and genomics programs. 298-299
- Christian M. Reidys, Fenix W. D. Huang, Jørgen E. Andersen, Robert C. Penner, Peter F. Stadler, Markus E. Nebel:
Addendum: topology and prediction of RNA pseudoknots. 300
Volume 28, Number 3, February 2012
- Xin Wei, Ann F. Hoffman, Shannon M. Hamilton, Qing Xiang, Yang He, W. Venus So, Sung-Sau So, David Mark:
A simple statistical test to infer the causality of target/phenotype correlation from small molecule phenotypic screens. 301-305
- Olga Shevchuk, Louisa Roselius, Gabriele Günther, Johannes Klein, Dieter Jahn, Michael Steinert, Richard Münch:
InFiRe - a novel computational method for the identification of insertion sites in transposon mutagenized bacterial genomes. 306-310
- David E. Larson, Christopher C. Harris, Ken Chen, Daniel C. Koboldt, Travis E. Abbott, David J. Dooling, Timothy J. Ley, Elaine R. Mardis, Richard K. Wilson, Li Ding:
SomaticSniper: identification of somatic point mutations in whole genome sequencing data. 311-317 - Antonio Marco, Sam Griffiths-Jones:
Detection of microRNAs in color space. 318-323
- Ryotaro Koike, Motonori Ota:
SCPC: a method to structurally compare protein complexes. 324-330 - Ke Chen, Marcin J. Mizianty, Lukasz A. Kurgan:
Prediction and analysis of nucleotide-binding residues using sequence and sequence-derived structural descriptors. 331-341 - Valdete M. Gonçalves-Almeida, Douglas E. V. Pires, Raquel Cardoso de Melo Minardi, Carlos Henrique da Silveira, Wagner Meira Jr., Marcelo M. Santoro:
HydroPaCe: understanding and predicting cross-inhibition in serine proteases through hydrophobic patch centroids. 342-349 - J. W. Heal, J. E. Jimenez-Roldan, Stephen A. Wells, R. B. Freedman, Rudolf A. Römer:
Inhibition of HIV-1 protease: the rigidity perspective. 350-357
- Gengxin Li, Joel Gelernter, Henry R. Kranzler, Hongyu Zhao:
M3: an improved SNP calling algorithm for Illumina BeadArray data. 358-365
- Wei Liu, Mahesan Niranjan:
Gaussian process modelling for bicoid mRNA regulation in spatio-temporal Bicoid profile. 366-372 - Alla Karnovsky, Terry E. Weymouth, Tim Hull, V. Glenn Tarcea, Giovanni Scardoni, Carlo Laudanna, Maureen A. Sartor, Kathleen A. Stringer, H. V. Jagadish, Charles F. Burant, Brian D. Athey, Gilbert S. Omenn:
Metscape 2 bioinformatics tool for the analysis and visualization of metabolomics and gene expression data. 373-380 - Kathrin Ballerstein, Axel von Kamp, Steffen Klamt, Utz-Uwe Haus:
Minimal cut sets in a metabolic network are elementary modes in a dual network. 381-387 - Mario Latendresse, Markus Krummenacker, Miles Trupp, Peter D. Karp:
Construction and completion of flux balance models from pathway databases. 388-396
- Natalia Jiménez-Lozano, Joan Segura, José Ramón Macías, Juanjo Vega, José María Carazo:
Integrating human and murine anatomical gene expression data for improved comparisons. 397-402 - Yupeng Wang, Sandeep J. Joseph, Xinyu Liu, Michael Kelley, Romdhane Rekaya:
SNPxGE2: a database for human SNP-coexpression associations. 403-410 - Nestor Milyaev, David Osumi-Sutherland, Simon Reeve, Nicholas Burton, Richard A. Baldock, J. Douglas Armstrong:
The Virtual Fly Brain browser and query interface. 411-415
- Yongbing Zhao, Jiayan Wu, Junhui Yang, Shixiang Sun, Jing-Fa Xiao, Jun Yu:
PGAP: pan-genomes analysis pipeline. 416-418 - Mikhail G. Dozmorov, Lukas R. Cara, Cory B. Giles, Jonathan D. Wren:
GenomeRunner: automating genome exploration. 419-420 - F. Anthony San Lucas, Gao T. Wang, Paul Scheet, Bo Peng:
Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant tools. 421-422 - Valentina Boeva, Tatiana G. Popova, Kevin Bleakley, Pierre Chiche, Julie Cappo, Gudrun Schleiermacher, Isabelle Janoueix-Lerosey, Olivier Delattre, Emmanuel Barillot:
Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data. 423-425
- Carlos Prieto, Carlos García-Estrada, Diego Lorenzana, Juan Francisco Martín:
NRPSsp: non-ribosomal peptide synthase substrate predictor. 426-427 - Benjamin Kreck, George Marnellos, Julia Richter, Felix Krueger, Reiner Siebert, Andre Franke:
B-SOLANA: an approach for the analysis of two-base encoding bisulfite sequencing data. 428-429 - Yuanxin Xi, Christoph Bock, Fabian Müller, Deqiang Sun, Alexander Meissner, Wei Li:
RRBSMAP: a fast, accurate and user-friendly alignment tool for reduced representation bisulfite sequencing. 430-432 - Robert Schmieder, Yan Wei Lim, Robert A. Edwards:
Identification and removal of ribosomal RNA sequences from metatranscriptomes. 433-435 - Antonio González, Jesse Stombaugh, Christian L. Lauber, Noah Fierer, Rob Knight:
SitePainter: a tool for exploring biogeographical patterns. 436-438
- Conan K. Wang, Saroja K. Weeratunga, Chris M. Pacheco, Andreas Hofmann:
DMAN: a Java tool for analysis of multi-well differential scanning fluorimetry experiments. 439-440 - Julia T. Philip, Charles H. Pence, Holly V. Goodson:
MTBindingSim: simulate protein binding to microtubules. 441-443
- Christian Fuchsberger, Daniel Taliun, Peter P. Pramstaller, Cristian Pattaro:
GWAtoolbox: an R package for fast quality control and handling of genome-wide association studies meta-analysis data. 444-445
- Enrico Glaab, Reinhard Schneider:
PathVar: analysis of gene and protein expression variance in cellular pathways using microarray data. 446-447
- Sarala M. Wimalaratne, Pierre Grenon, Robert Hoehndorf, Georgios V. Gkoutos, Bernard de Bono:
An infrastructure for ontology-based information systems in biomedicine: RICORDO case study. 448-450 - Kai Xia, Andrey A. Shabalin, Shunping Huang, Vered Madar, Yi-Hui Zhou, Wei Wang, Fei Zou, Wei Sun, Patrick F. Sullivan, Fred A. Wright:
seeQTL: a searchable database for human eQTLs. 451-452
Volume 28, Number 4, February 2012
- Wilson Wen Bin Goh, Hirotaka Oikawa, Judy Chia Ghee Sng, Marek J. Sergot, Limsoon Wong:
The role of miRNAs in complex formation and control. 453-456
- Thomas J. Hardcastle, Krystyna A. Kelly, David C. Baulcombe:
Identifying small interfering RNA loci from high-throughput sequencing data. 457-463 - Tim Carver, Simon R. Harris, Matthew Berriman, Julian Parkhill, Jacqueline A. McQuillan:
Artemis: an integrated platform for visualization and analysis of high-throughput sequence-based experimental data. 464-469 - Alberto Magi, Lorenzo Tattini, Tommaso Pippucci, Francesca Torricelli, Matteo Benelli:
Read count approach for DNA copy number variants detection. 470-478
- Yanju Zhang, Eric-Wubbo Lameijer, Peter A. C. 't Hoen, Zemin Ning, P. Eline Slagboom, Kai Ye:
PASSion: a pattern growth algorithm-based pipeline for splice junction detection in paired-end RNA-Seq data. 479-486 - Phil Arnold, Ionas Erb, Mikhail Pachkov, Nacho Molina, Erik van Nimwegen:
MotEvo: integrated Bayesian probabilistic methods for inferring regulatory sites and motifs on multiple alignments of DNA sequences. 487-494 - Benjamin P. Blackburne, Simon Whelan:
Measuring the distance between multiple sequence alignments. 495-502
- Ian Walsh, Alberto J. M. Martin, Tomás Di Domenico, Silvio C. E. Tosatto:
ESpritz: accurate and fast prediction of protein disorder. 503-509 - Tim Harder, Mikael Borg, Wouter Boomsma, Peter Røgen, Thomas Hamelryck:
Fast large-scale clustering of protein structures using Gauss integrals. 510-515 - Sikander Hayat, Arne Elofsson:
BOCTOPUS: improved topology prediction of transmembrane β barrel proteins. 516-522 - Sudhakar Sahoo, Andreas Alexander Albrecht:
Approximating the set of local minima in partial RNA folding landscapes. 523-530
- Tiejun Tong, Liang Chen, Hongyu Zhao:
Improved mean estimation and its application to diagonal discriminant analysis. 531-537 - Isaac S. Kohane, Vladimir I. Valtchinov:
Quantifying the white blood cell transcriptome as an accessible window to the multiorgan transcriptome. 538-545
- Lipi R. Acharya, Thair Judeh, Guangdi Wang, Dongxiao Zhu:
Optimal structural inference of signaling pathways from unordered and overlapping gene sets. 546-556 - Thomas Handorf, Edda Klipp:
Modeling mechanistic biological networks: An advanced Boolean approach. 557-563
- Youting Sun, Jianqiu Zhang, Ulisses M. Braga-Neto, Edward R. Dougherty:
BPDA2d - a 2D global optimization-based Bayesian peptide detection algorithm for liquid chromatograph-mass spectrometry. 564-572 - Raivo Kolde, Sven Laur, Priit Adler, Jaak Vilo:
Robust rank aggregation for gene list integration and meta-analysis. 573-580
- Leila Taher, Leelavati Narlikar, Ivan Ovcharenko:
CLARE: Cracking the LAnguage of Regulatory Elements. 581-583
- Thilo Muth, Juan A. García-Martín, Antonio Rausell, David de Juan, Alfonso Valencia, Florencio Pazos:
JDet: interactive calculation and visualization of function-related conservation patterns in multiple sequence alignments and structures. 584-586 - Jinyan Huang, Victor Renault, J. Sengenès, Nizar Touleimat, Sven Michel, Mark G. Lathrop, Jorg Tost:
MeQA: a pipeline for MeDIP-seq data quality assessment and analysis. 587-588 - Evarist Planet, Camille Stephan-Otto Attolini, Oscar Reina, Oscar Flores, David Rossell:
htSeqTools: high-throughput sequencing quality control, processing and visualization in R. 589-590 - Athina Theodosiou, Vasilis J. Promponas:
LaTcOm: a web server for visualizing rare codon clusters in coding sequences. 591-592 - Weichun Huang, Leping Li, Jason R. Myers, Gabor T. Marth:
ART: a next-generation sequencing read simulator. 593-594
- Miquel Ràmia, Pablo Librado, Sònia Casillas, Julio Rozas, Antonio Barbadilla:
PopDrowser: the Population Drosophila Browser. 595-596
- Sun Kim, Dongseop Kwon, Soo-Yong Shin, W. John Wilbur:
PIE the search: searching PubMed literature for protein interaction information. 597-598 - Jamie K. Teer, Eric D. Green, James C. Mullikin, Leslie G. Biesecker:
VarSifter: Visualizing and analyzing exome-scale sequence variation data on a desktop computer. 599-600
- Christian Schaefer, Alice Meier, Burkhard Rost, Yana Bromberg:
SNPdbe: constructing an nsSNP functional impacts database. 601-602
Volume 28, Number 5, March 2012
- Natasha Latysheva, Vivien L. Junker, William J. Palmer, Geoffrey A. Codd, Daniel Barker:
The evolution of nitrogen fixation in cyanobacteria. 603-606
- Maria D. Chikina, Olga G. Troyanskaya:
An effective statistical evaluation of ChIPseq dataset similarity. 607-613 - Katelyn McNair, Barbara A. Bailey, Robert A. Edwards:
PHACTS, a computational approach to classifying the lifestyle of phages. 614-618 - Anne-Katrin Emde, Marcel H. Schulz, David Weese, Ruping Sun, Martin Vingron, Vera M. Kalscheuer, Stefan A. Haas, Knut Reinert:
Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. 619-627
- Raymond Wan, Vo Ngoc Anh, Kiyoshi Asai:
Transformations for the compression of FASTQ quality scores of next-generation sequencing data. 628-635 - Søren Mørk, Ian H. Holmes:
Evaluating bacterial gene-finding HMM structures as probabilistic logic programs. 636-642 - Na You, Gabriel H. Murillo, Xiaoquan Su, Xiaowei Zeng, Jian Xu, Kang Ning, Shoudong Zhang, Jiankang Zhu, Xinping Cui:
SNP calling using genotype model selection on high-throughput sequencing data. 643-650 - Ergun Gumus, Olcay Kursun, Ahmet Sertbas, Duran Üstek:
Application of canonical correlation analysis for identifying viral integration preferences. 651-655 - Jonathan Göke, Marcel H. Schulz, Julia Lasserre, Martin Vingron:
Estimation of pairwise sequence similarity of mammalian enhancers with word neighbourhood counts. 656-663
- Zhe Zhang, Lin Wang, Yang Gao, Jie Zhang, Maxim Zhenirovskyy, Emil Alexov:
Predicting folding free energy changes upon single point mutations. 664-671
- Maxime Garcia, Raphaelle Millat-Carus, François Bertucci, Pascal Finetti, Daniel Birnbaum, Ghislain Bidaut:
Interactome-transcriptome integration for predicting distant metastasis in breast cancer. 672-678
- Alex L. B. Leach, James P. J. Chong, Kelly R. Redeker:
SSuMMo: rapid analysis, comparison and visualization of microbial communities. 679-686
- Serguei Sokol, Pierre Millard, Jean-Charles Portais:
influx_s: increasing numerical stability and precision for metabolic flux analysis in isotope labelling experiments. 687-693 - Kakajan Komurov:
Modeling community-wide molecular networks of multicellular systems. 694-700 - Mei-Ju May Chen, Lih-Ching Chou, Tsung-Ting Hsieh, Ding-Dar Lee, Kai-Wei Liu, Chi-Yuan Yu, Yen-Jen Oyang, Huai-Kuang Tsai, Chien-Yu Chen:
De novo motif discovery facilitates identification of interactions between transcription factors in Saccharomyces cerevisiae. 701-708
- Christian Senger, Björn A. Grüning, Anika Erxleben, Kersten Döring, Hitesh Patel, Stephan Flemming, Irmgard Merfort, Stefan Günther:
Mining and evaluation of molecular relationships in literature. 709-714
- Todd F. DeLuca, Jike Cui, Jae-Yoon Jung, Kristian Che St. Gabriel, Dennis P. Wall:
Roundup 2.0: enabling comparative genomics for over 1800 genomes. 715-716 - Thomas Hentrich, Julia M. Schulze, Eldon Emberly, Michael S. Kobor:
CHROMATRA: a Galaxy tool for visualizing genome-wide chromatin signatures. 717-718 - Gary K. Chen:
A scalable and portable framework for massively parallel variable selection in genetic association studies. 719-720 - Dongwan Hong, Arang Rhie, Sung-Soo Park, Jongkeun Lee, Young Seok Ju, Sujung Kim, Saet-Byeol Yu, Thomas Bleazard, Hyun Seok Park, Hwanseok Rhee, Hyonyong Chong, Kap-Seok Yang, Yeon-Su Lee, In-Hoo Kim, Jin Soo Lee, Jong-Il Kim, Jeong-Sun Seo:
FX: an RNA-Seq analysis tool on the cloud. 721-723 - Vladimir Makarov, Tina O'Grady, Guiqing Cai, Jayon Lihm, Joseph D. Buxbaum, Seungtai Yoon:
AnnTools: a comprehensive and versatile annotation toolkit for genomic variants. 724-725
- Thomas W. Chittenden, Eleanor Howe, Jennifer M. Taylor, Jessica Cara Mar, Martin J. Aryee, Harold Gómez, Razvan Sultana, John C. Braisted, Sarita J. Nair, John Quackenbush, Chris Holmes:
nEASE: a method for gene ontology subclassification of high-throughput gene expression data. 726-728 - Dan Wang, Li Yan, Qiang Hu, Lara E. Sucheston, Michael J. Higgins, Christine B. Ambrosone, Candace S. Johnson, Dominic J. Smiraglia, Song Liu:
IMA: an R package for high-throughput analysis of Illumina's 450K Infinium methylation data. 729-730
- Michal Komorowski, Justina Zurauskiene, Michael P. H. Stumpf:
StochSens - matlab package for sensitivity analysis of stochastic chemical systems. 731-733 - Rogan Carr, Elhanan Borenstein:
NetSeed: a network-based reverse-ecology tool for calculating the metabolic interface of an organism with its environment. 734-735 - Christoph Bueschl, Bernhard Kluger, Franz Berthiller, Gerald Lirk, Stephan Winkler, Rudolf Krska, Rainer Schuhmacher:
MetExtract: a new software tool for the automated comprehensive extraction of metabolite-derived LC/MS signals in metabolomics research. 736-738
- Sergey Kozhenkov, Michael Baitaluk:
Mining and integration of pathway diagrams from imaging data. 739-742 - Adrian Benton, John H. Holmes, Shawndra Hill, Annie Chung, Lyle H. Ungar:
medpie: an information extraction package for medical message board posts. 743-744 - Yasubumi Sakakibara, Tsuyoshi Hachiya, Miho Uchida, Nobuyoshi Nagamine, Yohei Sugawara, Masahiro Yokota, Masaomi Nakamura, Kris Popendorf, Takashi Komori, Kengo Sato:
COPICAT: a software system for predicting interactions between proteins and chemical compounds. 745-746
- Sentil Balaji, Charles Mcclendon, Rajesh Chowdhary, Jun S. Liu, Jinfeng Zhang:
IMID: integrated molecular interaction database. 747-749 - Mustafa H. Syed, Tatiana V. Karpinets, Morey Parang, Michael R. Leuze, Byung-Hoon Park, Doug Hyatt, Steven D. Brown, Steve Moulton, Michael D. Galloway, Edward C. Uberbacher:
BESC knowledgebase public portal. 750-751 - David van der Spoel, Paul J. van Maaren, Carl Caleman:
GROMACS molecule & liquid database. 752-753
Volume 28, Number 6, March 2012
- Charles C. Berry, Nicolas A. Gillet, Anat Melamed, Niall A. Gormley, Charles R. M. Bangham, Frederic D. Bushman:
Estimating abundances of retroviral insertion sites from DNA fragment length data. 755-762 - Santi González, Bàrbara Montserrat-Sentís, Friman Sánchez, Montserrat Puiggròs, Enrique Blanco, Alex Ramírez, David Torrents:
ReLA, a local alignment search tool for the identification of distal and proximal gene regulatory regions and their conserved transcription factor binding sites. 763-770
- Martin Reczko, Manolis Maragkakis, Panagiotis Alexiou, Ivo Grosse, Artemis G. Hatzigeorgiou:
Functional microRNA targets in protein coding sequences. 771-776 - Eva E. R. Philipp, Lars Kraemer, D. Mountfort, M. Schilhabel, Stefan Schreiber, Philip Rosenstiel:
The Transcriptome Analysis and Comparison Explorer - T-ACE: a platform-independent, graphical tool to process large RNAseq datasets of non-model organisms. 777-783
- David Ryan Koes, Carlos J. Camacho:
Small-molecule inhibitor starting points learned from protein-protein interaction inhibitor structure. 784-791 - Matthew G. Seetin, David H. Mathews:
TurboKnot: rapid prediction of conserved RNA secondary structures including pseudoknots. 792-798
- Sutirtha Chakraborty, Somnath Datta, Susmita Datta:
Surrogate variable analysis using partial least squares (SVA-PLS) in gene expression studies. 799-806 - Yihan Li, Debashis Ghosh:
Assumption weighting for incorporating heterogeneity into meta-analysis of genomic data. 807-814 - Kyungpil Kim, Keni Jiang, Siew Leng Teng, Lewis J. Feldman, Haiyan Huang:
Using biologically interrelated experiments to identify pathway genes in Arabidopsis. 815-822 - Ka Yee Yeung, T. A. Gooley, A. Zhang, Adrian E. Raftery, J. P. Radich, V. G. Oehler:
Predicting relapse prior to transplantation in chronic myeloid leukemia by integrating expert knowledge and expression data. 823-830
- Christopher J. R. Illingworth, Ville Mustonen:
A method to infer positive selection from marker dynamics in an asexual population. 831-837 - Chul Joo Kang, Paul Marjoram:
Exact coalescent simulation of new haplotype data from existing reference haplotypes. 838-844 - Clara S. Tang, Manuel A. R. Ferreira:
A gene-based test of association using canonical correlation analysis. 845-850
- Martin Simonsen, Stefan Maetschke, Mark A. Ragan:
Automatic selection of reference taxa for protein-protein interaction prediction with phylogenetic profiling. 851-857 - Alfredo Rodríguez, David Sosa, Leda Torres, Bertha Molina, Sara Frías, Luis Mendoza:
A Boolean network model of the FA/BRCA pathway. 858-866
- Thanh Thieu, Sneha Joshi, Samantha Warren, Dmitry Korkin:
Literature mining of host-pathogen interactions: comparing feature-based supervised learning and language-based approaches. 867-875
- Matti Niemenmaa, Aleksi Kallio, André Schumacher, Petri Klemelä, Eija Korpelainen, Keijo Heljanko:
Hadoop-BAM: directly manipulating next generation sequencing data in the cloud. 876-877 - Chi-Man Liu, Thomas K. F. Wong, Edward Wu, Ruibang Luo, Siu-Ming Yiu, Yingrui Li, Bingqiang Wang, Chang Yu, Xiaowen Chu, Kaiyong Zhao, Ruiqiang Li, Tak Wah Lam:
SOAP3: ultra-fast GPU-based parallel alignment tool for short reads. 878-879
- Grzegorz Chojnowski, Janusz M. Bujnicki, Matthias Bochtler:
RIBER/DIBER: a software suite for crystal content analysis in the studies of protein-nucleic acid complexes. 880-881
- Jeffrey T. Leek, W. Evan Johnson, Hilary S. Parker, Andrew E. Jaffe, John D. Storey:
The sva package for removing batch effects and other unwanted variation in high-throughput experiments. 882-883 - Björn Schwalb, Daniel Schulz, Mai Sun, Benedikt Zacher, Sebastian Dümcke, Dietmar E. Martin, Patrick Cramer, Achim Tresch:
Measurement of genome-wide RNA synthesis and decay rates with Dynamic Transcriptome Analysis (DTA). 884-885
- Michael C. Turchin, Joel Hirschhorn:
Gencrypt: one-way cryptographic hashes to detect overlapping individuals across samples. 886-888
- Kumar Chandan, Martijn P. van Iersel, Mirit I. Aladjem, Kurt W. Kohn, Augustin Luna:
PathVisio-Validator: a rule-based validation plugin for graphical pathway notations. 889-890 - Matthew DeJongh, Benjamin Bockstege, Paul Frybarger, Nicholas L. Hazekamp, Joshua Kammeraad, Travis McGeehan:
CytoSEED: a Cytoscape plugin for viewing, manipulating and analyzing metabolic models created by the Model SEED. 891-892 - Aleksandar Stojmirovic, Alexander Bliskovsky, Yi-Kuo Yu:
CytoSaddleSum: a functional enrichment analysis plugin for Cytoscape based on sum-of-weights scores. 893-894
- Michael Hartung, Anika Groß, Erhard Rahm:
CODEX: exploration of semantic changes between ontology versions. 895-896 - Mehdi Pirooznia, Tao Wang, Dimitrios Avramopoulos, David Valle, Gareth Thomas, Richard L. Huganir, Fernando S. Goes, James B. Potash, Peter P. Zandi:
SynaptomeDB: an ontology-based knowledgebase for synaptic genes. 897-899
- Christophe Dessimoz, Toni Gabaldón, David S. Roos, Erik L. L. Sonnhammer, Javier Herrero:
Toward community standards in the quest for orthologs. 900-904
- Isaac S. Kohane, Vladimir I. Valtchinov:
Quantifying the white blood cell transcriptome as an accessible window to the multiorgan transcriptome. 905
Volume 28, Number 7, April 2012
- Andrew Roth, Jiarui Ding, Ryan D. Morin, Anamaria Crisan, Gavin Ha, Ryan Giuliany, Ali Bashashati, Martin Hirst, Gulisa Turashvili, Arusha Oloumi, Marco A. Marra, Sam Aparicio, Sohrab P. Shah:
JointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data. 907-913
- Zhi Liu, Ahmed Abbas, Bing-Yi Jing, Xin Gao:
WaVPeak: picking NMR peaks through wavelet-based smoothing and volume-based filtering. 914-920
- Daniel C. Jones, Walter L. Ruzzo, Xinxia Peng, Michael G. Katze:
A new approach to bias correction in RNA-Seq. 921-928 - Shuji Kawaguchi, Kei Iida, Erimi Harada, Kousuke Hanada, Akihiro Matsui, Masanori Okamoto, Kazuo Shinozaki, Motoaki Seki, Tetsuro Toyoda:
Positional correlation analysis improves reconstruction of full-length transcripts and alternative isoforms from noisy array signals or short reads. 929-937
- Degui Zhi, Jihua Wu, Nianjun Liu, Kui Zhang:
Genotype calling from next-generation sequencing data using haplotype information of reads. 938-946
- John L. Van Hemert, Julie A. Dickerson:
Discriminating response groups in metabolic and regulatory pathway networks. 947-954 - Shiwen Zhao, Shao Li:
A co-module approach for elucidating drug-disease associations and revealing their molecular basis. 955-961 - Andy C. W. Lai, Alex N. Nguyen Ba, Alan M. Moses:
Predicting kinase substrates using conservation of local motif density. 962-969 - Feng He, Jie Ren, Wei Wang, Jun Ma:
Evaluating the Drosophila Bicoid morphogen gradient system through dissecting the noise in transcriptional bursts. 970-975 - Robert J. Weatheritt, Katja Luck, Evangelia Petsalaki, Norman E. Davey, Toby J. Gibson:
The identification of short linear motif-mediated interfaces within the human interactome. 976-982 - Guy Naamati, Yitzhak Friedman, Ohad Balaga, Michal Linial:
Susceptibility of the human pathways graphs to fragmentation by small sets of microRNAs. 983-990
- Maria Liakata, Shyamasree Saha, Simon Dobnik, Colin R. Batchelor, Dietrich Rebholz-Schuhmann:
Automatic recognition of conceptualization zones in scientific articles and two life science applications. 991-1000 - Theofanis Karaletsos, Oliver Stegle, Christine Dreyer, John M. Winn, Karsten M. Borgwardt:
ShapePheno: unsupervised extraction of shape phenotypes from biological image collections. 1001-1008 - Nima Aghaeepour, Pratip K. Chattopadhyay, Anuradha Ganesan, Kieran O'Neill, Habil Zare, Adrin Jalali, Holger H. Hoos, Mario Roederer, Ryan Remy Brinkman:
Early immunologic correlates of HIV protection can be identified from computational analysis of complex multivariate T-cell flow cytometry assays. 1009-1016
- Anne Niknejad, Aurélie Comte, Gilles Parmentier, Julien Roux, Frederic B. Bastian, Marc Robinson-Rechavi:
vHOG, a multispecies vertebrate ontology of homologous organs groups. 1017-1020
- William K. M. Lai, Jonathan E. Bard, Michael J. Buck:
ArchTEx: accurate extraction and visualization of next-generation sequence data. 1021-1023 - Ruping Sun, Michael I. Love, Tomasz Zemojtel, Anne-Katrin Emde, Ho-Ryun Chung, Martin Vingron, Stefan A. Haas:
Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads. 1024-1025
- Conan K. Wang, Ursula Broder, Saroja K. Weeratunga, Robin B. Gasser, Alex Loukas, Andreas Hofmann:
SBAL: a practical tool to generate and edit structure-based amino acid sequence alignments. 1026-1027 - Sang-Mun Chi, Dougu Nam:
WegoLoc: accurate prediction of protein subcellular localization using weighted Gene Ontology terms. 1028-1030 - Kian Huat Lim, William G. Fairbrother:
Spliceman - a computational web server that predicts sequence variations in pre-mRNA splicing. 1031-1032 - Martin Wu, Alexandra J. Scott:
Phylogenomic analysis of bacterial and archaeal sequences with AMPHORA2. 1033-1034 - Raoul Jean Pierre Bonnal, Jan Aerts, George Githinji, Naohisa Goto, Daniel MacLean, Chase A. Miller, Hiroyuki Mishima, Massimiliano Pagani, Ricardo Ramirez-Gonzalez, Geert Smant, Francesco Strozzi, Rob Syme, Rutger A. Vos, Trevor J. Wennblom, Ben J. Woodcroft, Toshiaki Katayama, Pjotr Prins:
Biogem: an effective tool-based approach for scaling up open source software development in bioinformatics. 1035-1037
- Alessandro Barbato, Pascal Benkert, Torsten Schwede, Anna Tramontano, Jan Kosinski:
Improving your target-template alignment with MODalign. 1038-1039 - Franck Samson, Richard Shrager, Chin-Hsien Tai, Vichetra Sam, Byungkook Lee, Peter J. Munson, Jean-François Gibrat, Jean Garnier:
DOMIRE: a web server for identifying structural domains and their neighbors in proteins. 1040-1041
- Danny Arends, K. Joeri van der Velde, Pjotr Prins, Karl W. Broman, Steffen Möller, Ritsert C. Jansen, Morris A. Swertz:
xQTL workbench: a scalable web environment for multi-level QTL analysis. 1042-1044 - John Bunge, Linda Woodard, Dankmar Böhning, James A. Foster, Sean Connolly, Heather K. Allen:
Estimating population diversity with CatchAll. 1045-1047
- Darren J. Creek, Andris Jankevics, Karl E. V. Burgess, Rainer Breitling, Michael P. Barrett:
IDEOM: an Excel interface for analysis of LC-MS-based metabolomics data. 1048-1049 - Eero Lihavainen, Jarno Mäkelä, Johannes N. Spelbrink, Andre S. Ribeiro:
Mytoe: automatic analysis of mitochondrial dynamics. 1050-1051
- Till Bald, Johannes Barth, Anna Niehues, Michael Specht, Michael Hippler, Christian Fufezan:
pymzML - Python module for high-throughput bioinformatics on mass spectrometry data. 1052-1053
- Valentin Guignon, Gaëtan Droc, Michael Alaux, Franc-Christophe Baurens, Olivier Garsmeur, Claire Poiron, Tim Carver, Mathieu Rouard, Stéphanie Bocs:
Chado Controller: advanced annotation management with a community annotation system. 1054-1056
Volume 28, Number 8, April 2012
- Hanchuan Peng, Alex Bateman, Alfonso Valencia, Jonathan D. Wren:
Bioimage informatics: a new category in Bioinformatics. 1057
- William Ritchie, Dadi Gao, John E. J. Rasko:
Defining and providing robust controls for microRNA prediction. 1058-1061
- Dominik Beck, Miriam Brandl, Lies Boelen, Ashwin Unnikrishnan, John E. Pimanda, Jason W. H. Wong:
Signal analysis for genome-wide maps of histone modifications measured by ChIP-seq. 1062-1069
- Vitaly L. Galinsky:
YOABS: yet other aligner of biological sequences - an efficient linearly scaling nucleotide aligner. 1070-1077 - Vincent Miele, Simon Penel, Vincent Daubin, Franck Picard, Daniel Kahn, Laurent Duret:
High-quality sequence clustering guided by network topology and multiple alignment likelihood. 1078-1085 - Marcel H. Schulz, Daniel R. Zerbino, Martin Vingron, Ewan Birney:
Oases: robust de novo RNA-seq assembly across the dynamic range of expression levels. 1086-1092
- Hisanori Kiryu, Kiyoshi Asai:
Rchange: algorithms for computing energy changes of RNA secondary structures in response to base mutations. 1093-1101
- Ruijie Liu, Ana-Teresa Maia, Roslin Russell, Carlos Caldas, Bruce A. Ponder, Matthew E. Ritchie:
Allele-specific expression analysis methods for high-density SNP microarray data. 1102-1108 - Zhongxue Chen, Qingzhong Liu, Saralees Nadarajah:
A new statistical approach to detecting differentially methylated loci for case control Illumina array methylation data. 1109-1113 - Leonid Chindelevitch, Daniel Ziemek, Ahmed Enayetallah, Ranjit Randhawa, Ben Sidders, Christoph Brockel, Enoch S. Huang:
Causal reasoning on biological networks: interpreting transcriptional changes. 1114-1121 - Jeffrey T. Chang:
Deriving transcriptional programs and functional processes from gene expression databases. 1122-1129
- Joep Vanlier, Christian A. Tiemann, Peter A. J. Hilbers, Natal A. W. van Riel:
An integrated strategy for prediction uncertainty analysis. 1130-1135 - Joep Vanlier, Christian A. Tiemann, Peter A. J. Hilbers, Natal A. W. van Riel:
A Bayesian approach to targeted experiment design. 1136-1142
- Jan Kölling, Daniel Langenkämper, Sylvie Abouna, Michael Khan, Tim W. Nattkemper:
WHIDE - a web tool for visual data mining colocation patterns in multivariate bioimages. 1143-1150 - Loris Nanni, Sheryl Brahnam, Alessandra Lumini:
Combining multiple approaches for gene microarray classification. 1151-1157 - Seongho Kim, Imhoi Koo, Xiaoli Wei, Xiang Zhang:
A method of finding optimal weight factors for compound identification in gas chromatography-mass spectrometry. 1158-1163
- Xiaobei Zhao, Albin Sandelin:
GMD: measuring the distance between histograms with applications on high-throughput sequencing reads. 1164-1165 - Konstantin Okonechnikov, Olga Golosova, Mikhail Fursov:
Unipro UGENE: a unified bioinformatics toolkit. 1166-1167 - Volker Steiß, Thomas Letschert, Helmut Schäfer, Roman Pahl:
PERMORY-MPI: a program for high-speed parallel permutation testing in genome-wide association studies. 1168-1169
- Oscar Westesson, Lars Barquist, Ian H. Holmes:
HandAlign: Bayesian multiple sequence alignment, phylogeny and ancestral reconstruction. 1170-1171
- Yingjie Lin, Seungyeul Yoo, Roberto Sanchez:
SiteComp: a server for ligand binding site analysis in protein structures. 1172-1173
- Aparna Bhaduri, Kun Qu, Carolyn S. Lee, Alexander Ungewickell, Paul A. Khavari:
Rapid identification of non-human sequences in high-throughput sequencing datasets. 1174-1175
- Mathieu Gautier, Renaud Vitalis:
rehh: an R package to detect footprints of selection in genome-wide SNP data from haplotype structure. 1176-1177
- Johannes Gräßler, Dirk Koschützki, Falk Schreiber:
CentiLib: comprehensive analysis and exploration of network centralities. 1178-1179 - Richard R. Adams:
SED-ED, a workflow editor for computational biology experiments written in SED-ML. 1180-1181
- Hanwen Huang, Xiaosun Lu, Yufeng Liu, Perry Haaland, J. S. Marron:
R/DWD: distance-weighted discrimination for classification, visualization and batch adjustment. 1182-1183
- Markus Krupp, Jens U. Marquardt, Ugur Sahin, Peter R. Galle, John C. Castle, Andreas Teufel:
RNA-Seq Atlas - a reference database for gene expression profiling in normal tissue by next-generation sequencing. 1184-1185 - Nigel Collier, Son Doan:
GENI-DB: a database of global events for epidemic intelligence. 1186-1188 - Scott F. Saccone, Jiaxi Quan, Peter L. Jones:
BioQ: tracing experimental origins in public genomic databases using a novel data provenance model. 1189-1191
Volume 28, Number 9, May 2012
- Pablo Meyer, Julia Hoeng, John Jeremy Rice, Raquel Norel, Jörg Sprengel, Katrin Stolle, Thomas Bonk, Stephanie Corthesy, Ajay K. Royyuru, Manuel C. Peitsch, Gustavo Stolovitzky:
Industrial methodology for process verification in research (IMPROVER): toward systems biology verification. 1193-1201
- Iman Hajirasouliha, Alexander Schönhuth, David de Juan, Alfonso Valencia, Süleyman Cenk Sahinalp:
Mirroring co-evolving trees in the light of their topologies. 1202-1208
- Michael I. Sadowski, William R. Taylor:
Evolutionary inaccuracy of pairwise structural alignments. 1209-1215 - Noah M. Daniels, Raghavendra Hosur, Bonnie Berger, Lenore J. Cowen:
SMURFLite: combining simplified Markov random fields with simulated evolution improves remote homology detection for beta-structural proteins into the twilight zone. 1216-1222 - Bin Li, Feng Liang, Jianhua Hu, Xuming He:
Reno: regularized non-parametric analysis of protein lysate array data. 1223-1229
- William H. Mather, Jeff Hasty, Lev S. Tsimring:
Fast stochastic algorithm for simulating evolutionary population dynamics. 1230-1238
- Hang T. T. Phan, Michael J. E. Sternberg:
PINALOG: a novel approach to align protein interaction networks - implications for complex detection and function prediction. 1239-1245 - Yuan Yuan, Yanxun Xu, Jianfeng Xu, Robyn L. Ball, Han Liang:
Predicting the lethal phenotype of the knockout mouse by integrating comprehensive genomic data. 1246-1252
- David Campos, Sérgio Matos, Ian Lewin, José Luís Oliveira, Dietrich Rebholz-Schuhmann:
Harmonization of gene/protein annotations: towards a gold standard MEDLINE. 1253-1261
- David Osumi-Sutherland, Simon Reeve, Christopher J. Mungall, Fabian Neuhaus, Alan Ruttenberg, Gregory S. X. E. Jefferis, J. Douglas Armstrong:
A strategy for building neuroanatomy ontologies. 1262-1269
- Sabine Ménigaud, Ludovic Mallet, Géraldine Picord, Cécile Churlaud, Alexandre Borrel, Patrick Deschavanne:
GOHTAM: a website for 'Genomic Origin of Horizontal Transfers, Alignment and Metagenomics'. 1270-1271 - Jing-Woei Li, Robert Schmieder, R. Matthew Ward, Joann Delenick, Eric C. Olivares, David Mittelman:
SEQanswers: an open access community for collaboratively decoding genomes. 1272-1273 - Junhee Seok, Weihong Xu, Hong Gao, Ronald W. Davis, Wenzhong Xiao:
JETTA: junction and exon toolkits for transcriptome analysis. 1274-1275
- Kris Popendorf, Yasubumi Sakakibara:
SAMSCOPE: an OpenGL-based real-time interactive scale-free SAM viewer. 1276-1277
- Adam Hospital, Pau Andrio, Carlos Fenollosa, Damjan Cicin-Sain, Modesto Orozco, Josep Lluis Gelpí:
MDWeb and MDMoby: an integrated web-based platform for molecular dynamics simulations. 1278-1279
- Richard T. Barfield, Varun Kilaru, Alicia K. Smith, Karen N. Conneely:
CpGassoc: an R function for analysis of DNA methylation microarray data. 1280-1281 - Mark Reppell, Michael Boehnke, Sebastian Zöllner:
FTEC: a coalescent simulator for modeling faster than exponential growth. 1282-1283
- Florian Gnad, Javier Estrada, Jeremy Gunawardena:
Proteus: a web-based, context-specific modelling tool for molecular networks. 1284-1286 - Nicolae Radu Zabet, Boris Adryan:
GRiP: a computational tool to simulate transcription factor binding in prokaryotes. 1287-1289 - Stefan Streif, Anton Savchenko, Philipp Rumschinski, Steffen Borchers, Rolf Findeisen:
ADMIT: a toolbox for guaranteed model invalidation, estimation and qualitative-quantitative modeling. 1290-1291
- J. Lamar Barnett, Jialiang Yang, Zhipeng Cai, Tong Zhang, Xiu-Feng Wan:
AntigenMap 3D: an online antigenic cartography resource. 1292-1293 - Pierre Millard, Fabien Létisse, Serguei Sokol, Jean-Charles Portais:
IsoCor: correcting MS data in isotope labeling experiments. 1294-1296
- Catherine Stamoulis, Rebecca A. Betensky:
A novel signal processing approach for the detection of copy number variations in the human genome. 1297
Volume 28, Number 10, May 2012
- Cyril F. Reboul, Khalid Mahmood, James C. Whisstock, Michelle A. Dunstone:
Predicting giant transmembrane β-barrel architecture. 1299-1302
- Hiren J. Joshi, Katy M. Christiansen, Joffrey Fitz, Jun Cao, Anna Lipzen, Joel Martin, A. Michelle Smith-Moritz, Len A. Pennacchio, Wendy S. Schackwitz, Detlef Weigel, Joshua L. Heazlewood:
1001 Proteomes: a functional proteomics portal for the analysis of Arabidopsis thaliana accessions. 1303-1306
- Jason Li, Richard Lupat, Kaushalya C. Amarasinghe, Ella R. Thompson, Maria A. Doyle, Georgina L. Ryland, Richard W. Tothill, Saman K. Halgamuge, Ian G. Campbell, Kylie L. Gorringe:
CONTRA: copy number analysis for targeted resequencing. 1307-1313
- Jie Lin, Donald A. Adjeroh, Bing-Hua Jiang:
Probabilistic suffix array: efficient modeling and prediction of protein families. 1314-1323 - Matthew S. Burriesci, Erik M. Lehnert, John R. Pringle:
Fulcrum: condensing redundant reads from high-throughput sequencing studies. 1324-1327 - Erola Pairo, Joan Maynou, Santiago Marco, Alexandre Perera:
A subspace method for the detection of transcription factor binding sites. 1328-1335 - Hongtao Sun, Jeremy D. Buhler:
PhyLAT: a phylogenetic local alignment tool. 1336-1344
- Bin Pang, Nan Zhao, Dmitry Korkin, Chi-Ren Shyu:
Fast protein binding site comparisons using visual words representation. 1345-1352
- Andrey A. Shabalin:
Matrix eQTL: ultra fast eQTL analysis via large matrix operations. 1353-1358
- Yael Baran, Bogdan Pasaniuc, Sriram Sankararaman, Dara G. Torgerson, Christopher Gignoux, Celeste Eng, William Rodriguez-Cintron, Rocio Chapela, Jean G. Ford, Pedro C. Avila, Jose Rodriguez-Santana, Esteban Gonzàlez Burchard, Eran Halperin:
Fast and accurate inference of local ancestry in Latino populations. 1359-1367 - Hokeun Sun, Shuang Wang:
Penalized logistic regression for high-dimensional DNA methylation data with case-control studies. 1368-1375
- Robert Küffner, Tobias Petri, Pegah Tavakkolkhah, Lukas Windhager, Ralf Zimmer:
Inferring gene regulatory networks by ANOVA. 1376-1382
- Haixuan Yang, Tamás Nepusz, Alberto Paccanaro:
Improving GO semantic similarity measures by exploring the ontology beneath the terms and modelling uncertainty. 1383-1389 - Andrew Sparkes, Amanda Clare:
AutoLabDB: a substantial open source database schema to support a high-throughput automated laboratory. 1390-1397
- Nizar Fawal, Bruno Savelli, Christophe Dunand, Catherine Mathé:
GECA: a fast tool for gene evolution and conservation analysis in eukaryotic protein families. 1398-1399
- Federico Comoglio, Maurizio Rinaldi:
Rknots: topological analysis of knotted biopolymers with R. 1400-1401
- Vincent Xue, Tony Burdett, Margus Lukk, Julie Taylor, Alvis Brazma, Helen E. Parkinson:
MageComet - web application for harmonizing existing large-scale experiment descriptions. 1402-1403 - Penghao Wang, Pengyi Yang, Jean Yee Hwa Yang:
OCAP: an open comprehensive analysis pipeline for iTRAQ. 1404-1405
- Mario Novkovic, Juraj Simunic, Viktor Bojovic, Alessandro Tossi, Davor Juretic:
DADP: the database of anuran defense peptides. 1406-1407 - Maureen A. Sartor, Alexander S. Ade, Zach Wright, David J. States, Gilbert S. Omenn, Brian D. Athey, Alla Karnovsky:
Metab2MeSH: annotating compounds with medical subject headings. 1408-1410 - Bo Qin, Meng Zhou, Ying Ge, Len Taing, Tao Liu, Qian Wang, Su Wang, Junsheng Chen, Lingling Shen, Xikun Duan, Sheng'en Hu, Wei Li, Henry Long, Yong Zhang, Xiaole Shirley Liu:
CistromeMap: a knowledgebase and web server for ChIP-Seq and DNase-Seq studies in mouse and human. 1411-1412
- Feng Feng, Ana Paula Sales, Thomas B. Kepler:
A Bayesian approach for estimating calibration curves and unknown concentrations in immunoassays. 1413
Volume 28, Number 11, June 2012
- Anthony J. Cox, Markus J. Bauer, Tobias Jakobi, Giovanna Rosone:
Large-scale compression of genomic sequence databases with the Burrows-Wheeler transform. 1415-1419
- Yu Peng, Henry C. M. Leung, Siu-Ming Yiu, Francis Y. L. Chin:
IDBA-UD: a de novo assembler for single-cell and metagenomic sequencing data with highly uneven depth. 1420-1428 - Alexey A. Gritsenko, Jurgen F. Nijkamp, Marcel J. T. Reinders, Dick de Ridder:
GRASS: a generic algorithm for scaffolding next-generation sequencing assemblies. 1429-1437
- Matthieu Chartier, Francis Gaudreault, Rafael Najmanovich:
Large-scale analysis of conserved rare codon clusters suggests an involvement in co-translational molecular recognition events. 1438-1445 - Anton Aboukhalil, Martha L. Bulyk:
LOESS correction for length variation in gene set-based genomic sequence analysis. 1446-1454 - Binbin Lai, Ruogu Ding, Yang Li, Liping Duan, Huaiqiu Zhu:
A de novo metagenomic assembly program for shotgun DNA reads. 1455-1462
- Valéry Ozenne, Frédéric Bauer, Loïc Salmon, Jie-rong Huang, Malene Ringkjøbing Jensen, Stéphane Segard, Pau Bernadó, Céline Charavay, Martin Blackledge:
Flexible-meccano: a tool for the generation of explicit ensemble descriptions of intrinsically disordered proteins and their associated experimental observables. 1463-1470
- Christian Otto, Kristin Reiche, Jörg Hackermüller:
Detection of differentially expressed segments in tiling array data. 1471-1479 - Haroon Naeem, Ralf Zimmer, Pegah Tavakkolkhah, Robert Küffner:
Rigorous assessment of gene set enrichment tests. 1480-1486 - Andrew E. Teschendorff, Martin Widschwendter:
Differential variability improves the identification of cancer risk markers in DNA methylation studies profiling precursor cancer lesions. 1487-1494
- Jochen Weile, Katherine James, Jennifer Hallinan, Simon J. Cockell, Phillip W. Lord, Anil Wipat, Darren J. Wilkinson:
Bayesian integration of networks without gold standards. 1495-1500 - Xin Liu, Mahesan Niranjan:
State and parameter estimation of the heat shock response system using Kalman and particle filters. 1501-1507 - Bing Liu, Andrei Hagiescu, Sucheendra K. Palaniappan, Bipasa Chattopadhyay, Zheng Cui, Weng-Fai Wong, P. S. Thiagarajan:
Approximate probabilistic analysis of biopathway dynamics. 1508-1516 - Nicolae Radu Zabet, Boris Adryan:
A comprehensive computational model of facilitated diffusion in prokaryotes. 1517-1524
- Simon P. Sadedin, Bernard J. Pope, Alicia Oshlack:
Bpipe: a tool for running and managing bioinformatics pipelines. 1525-1526 - Vikas Rao Pejaver, Jaehyun An, SungMin Rhee, Ankita Bhan, Jeong-Hyeon Choi, Boshu Liu, Heewook Lee, Pamela J. Brown, David Kysela, Yves V. Brun, Sun Kim:
GeneclusterViz: a tool for conserved gene cluster visualization, exploration and analysis. 1527-1529 - David S. DeLuca, Joshua Z. Levin, Andrey Sivachenko, Tim Fennell, Marc-Danie Nazaire, Chris Williams, Michael Reich, Wendy Winckler, Gad Getz:
RNA-SeQC: RNA-seq metrics for quality control and process optimization. 1530-1532
- Xuesong Hu, Jianying Yuan, Yujian Shi, Jianliang Lu, Binghang Liu, Zhenyu Li, Yanxiang Chen, Desheng Mu, Hao Zhang, Nan Li, Zhen Yue, Fan Bai, Heng Li, Wei Fan:
pIRS: Profile-based Illumina pair-end reads simulator. 1533-1535
- Andrei-Alin Popescu, Katharina T. Huber, Emmanuel Paradis:
ape 3.0: New tools for distance-based phylogenetics and evolutionary analysis in R. 1536-1537
- Osvaldo A. Martin, Jorge A. Vila, Harold A. Scheraga:
CheShift-2: graphic validation of protein structures. 1538-1539 - Emilie Pihan, Lionel Colliandre, Jean-François Guichou, Dominique Douguet:
e-Drug3D: 3D structure collections dedicated to drug repurposing and fragment-based drug design. 1540-1541
- Laurent Jourdren, Maria Bernard, Marie-Agnès Dillies, Stéphane Le Crom:
Eoulsan: a cloud computing-based framework facilitating high throughput sequencing analyses. 1542-1543 - Jian-Bo Pan, Shi-chang Hu, Hao Wang, Quan Zou, Zhi-Liang Ji:
PaGeFinder: quantitative identification of spatiotemporal pattern genes. 1544-1545 - Daryl Waggott, Kenneth C. Chu, Shaoming Yin, Bradly G. Wouters, Fei-Fei Liu, Paul C. Boutros:
NanoStringNorm: an extensible R package for the pre-processing of NanoString mRNA and miRNA data. 1546-1548
- Gábor Szederkényi, Julio R. Banga, Antonio A. Alonso:
CRNreals: a toolbox for distinguishability and identifiability analysis of biochemical reaction networks. 1549-1550
- Feng Gao, Hao Luo, Chun-Ting Zhang:
DeOri: a database of eukaryotic DNA replication origins. 1551-1552
- Stephen A. Stanhope, Mark Abney:
GLOGS: a fast and powerful method for GWAS of binary traits with risk covariates in related populations. 1553-1554
Volume 28, Number 12, June 2012
- Bonnie Berger:
Editorial. 1 - ISMB 2012 Committee. 2-6
- Alexander Herbig, Günter Jäger, Florian Battke, Kay Nieselt:
GenomeRing: alignment visualization based on SuperGenome coordinates. 7-15 - Xiao Cai, Hua Wang, Heng Huang, Chris H. Q. Ding:
Joint stage recognition and anatomical annotation of drosophila gene expression patterns. 16-24 - Linqing Feng, Ting Zhao, Jinhyun Kim:
Improved synapse detection for mGRASP-assisted brain connectivity mapping. 25-31 - Jieyue Li, Liang Xiong, Jeff G. Schneider, Robert F. Murphy:
Protein subcellular location pattern classification in cellular images using latent discriminative models. 32-39 - Yongjin Park, Joel S. Bader:
How networks change with time. 40-48 - Yu-Keng Shih, Srinivasan Parthasarathy:
A single source k-shortest paths algorithm to infer regulatory pathways in a gene network. 49-58 - Jianzhu Ma, Jian Peng, Sheng Wang, Jinbo Xu:
A conditional neural fields model for protein threading. 59-66 - Milana Frenkel-Morgenstern, Alfonso Valencia:
Novel domain combinations in proteins encoded by chimeric transcripts. 67-74 - Fatemeh Miri Disfani, Wei-Lun Hsu, Marcin J. Mizianty, Christopher J. Oldfield, Bin Xue, A. Keith Dunker, Vladimir N. Uversky, Lukasz A. Kurgan:
MoRFpred, a computational tool for sequence-based prediction and characterization of short disorder-to-order transitioning binding regions in proteins. 75-83 - Ryan G. Christensen, Metewo Selase Enuameh, Marcus B. Noyes, Michael H. Brodsky, Scot A. Wolfe, Gary D. Stormo:
Recognition models to predict DNA-binding specificities of homeodomain proteins. 84-89 - Sikander Hayat, Arne Elofsson:
Ranking models of transmembrane β-barrel proteins using Z-coordinate predictions. 90-96 - Arun Siddharth Konagurthu, Arthur M. Lesk, Lloyd Allison:
Minimum message length inference of secondary structure from protein coordinate data. 97-105 - Dorit S. Hochbaum, Chun-Nan Hsu, Yan T. Yang:
Ranking of multidimensional drug profiling data by fractional-adjusted bi-partitional scores. 106-114 - Atsushi Niida, Seiya Imoto, Teppei Shimamura, Satoru Miyano:
Statistical model-based testing to evaluate the recurrence of genomic aberrations. 115-120 - Chirag J. Patel, Rong Chen, Atul J. Butte:
Data-driven integration of epidemiological and toxicological data to select candidate interacting genes and environmental factors in association with disease. 121-126 - Hua Wang, Feiping Nie, Heng Huang, Shannon L. Risacher, Andrew J. Saykin, Li Shen:
Identifying disease sensitive and quantitative trait-relevant biomarkers from multidimensional heterogeneous imaging genetics data via sparse multimodal multitask learning. 127-136 - Seunghak Lee, Eric P. Xing:
Leveraging input and output structures for joint mapping of epistatic and marginal eQTLs. 137-146 - Gregory Darnell, Dat Duong, Buhm Han, Eleazar Eskin:
Incorporating prior information into association studies. 147-153 - Derek Aguiar, Bjarni V. Halldórsson, Eric M. Morrow, Sorin Istrail:
DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism. 154-162 - Qian Peng, Joseph R. Ecker:
Detection of allele-specific methylation through a generalized heterogeneous epigenome model. 163-171 - Thomas C. Conway, Jeremy Wazny, Andrew J. Bromage, Martin Tymms, Dhanya Sooraj, Elizabeth D. Williams, Bryan Beresford-Smith:
Xenome - a tool for classifying reads from xenograft samples. 172-178 - Deniz Yörükoglu, Faraz Hach, Lucas Swanson, Colin C. Collins, Inanç Birol, Süleyman Cenk Sahinalp:
Dissect: detection and characterization of novel structural alterations in transcribed sequences. 179-187 - Roy Ronen, Christina Boucher, Hamidreza Chitsaz, Pavel A. Pevzner:
SEQuel: improving the accuracy of genome assemblies. 188-196 - David Golan, Yaniv Erlich, Saharon Rosset:
Weighted pooling - practical and cost-effective techniques for pooled high-throughput sequencing. 197-206 - Vladimir Reinharz, François Major, Jérôme Waldispühl:
Towards 3D structure prediction of large RNA molecules: an integer programming framework to insert local 3D motifs in RNA secondary structure. 207-214 - Jan Hoinka, Elena Zotenko, Adam Friedman, Zuben E. Sauna, Teresa M. Przytycka:
Identification of sequence-structure RNA binding motifs for SELEX-derived aptamers. 215-223 - Steffen Heyne, Fabrizio Costa, Dominic Rose, Rolf Backofen:
GraphClust: alignment-free structural clustering of local RNA secondary structures. 224-232 - Christopher A. Penfold, Vicky Buchanan-Wollaston, Katherine J. Denby, David L. Wild:
Nonparametric Bayesian inference for perturbed and orthologous gene regulatory networks. 233-241 - Anton Polishko, Nadia Ponts, Karine G. Le Roch, Stefano Lonardi:
NOrMAL: accurate nucleosome positioning using a modified Gaussian mixture model. 242-249 - Tatsunori B. Hashimoto, Tommi S. Jaakkola, Richard Sherwood, Esteban O. Mazzoni, Hynek Wichterle, David K. Gifford:
Lineage-based identification of cellular states and expression programs. 250-257 - Aaron Wise, Zoltán N. Oltvai, Ziv Bar-Joseph:
Matching experiments across species using expression values and textual information. 258-264 - Franziska Hufsky, Kai Dührkop, Florian Rasche, Markus Chimani, Sebastian Böcker:
Fast alignment of fragmentation trees. 265-273 - Serita M. Nelesen, Kevin Liu, Li-San Wang, C. Randal Linder, Tandy J. Warnow:
DACTAL: divide-and-conquer trees (almost) without alignments. 274-282 - Mukul S. Bansal, Eric J. Alm, Manolis Kellis:
Efficient algorithms for the reconciliation problem with gene duplication, horizontal transfer and loss. 283-291 - Götz Fabian, Thomas Wächter, Michael Schroeder:
Extending ontologies by finding siblings using set expansion techniques. 292-300
- Ahrim Youn, Richard Simon:
Estimating the order of mutations during tumorigenesis from tumor genome sequencing data. 1555-1561 - Tuobin Wang, Arminja N. Kettenbach, Scott A. Gerber, Chris Bailey-Kellogg:
MMFPh: a maximal motif finder for phosphoproteomics datasets. 1562-1570 - Axel Bernal, Koby Crammer, Fernando Pereira:
Automated gene-model curation using global discriminative learning. 1571-1578 - Zhong-Ru Xie, Ming-Jing Hwang:
Ligand-binding site prediction using ligand-interacting and binding site-enriched protein triangles. 1579-1585 - Xuan Wang, Gordon A. Anderson, Richard D. Smith, Alan R. Dabney:
A hybrid approach to protein differential expression in mass spectrometry-based proteomics. 1586-1591 - Ovidiu D. Iancu, Sunita Kawane, Daniel Bottomly, Robert P. Searles, Robert Hitzemann, Shannon K. McWeeney:
Utilizing RNA-Seq data for de novo coexpression network inference. 1592-1597 - T. S. Shah, Jimmy Zhenli Liu, J. A. B. Floyd, James A. Morris, N. Wirth, Jeffrey C. Barrett, Carl A. Anderson:
optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants. 1598-1603 - Bor-Sen Chen, Chia-Chou Wu:
On the calculation of signal transduction ability of signaling transduction pathways in intracellular communication: systematic approach. 1604-1611 - Juliane Siebourg, Gunter Merdes, Benjamin Misselwitz, Wolf-Dietrich Hardt, Niko Beerenwinkel:
Stability of gene rankings from RNAi screens. 1612-1618 - Dennis Egen, Desmond S. Lun:
Truncated branch and bound achieves efficient constraint-based genetic design. 1619-1623 - Tavis K. Anderson, William W. Laegreid, Francesco Cerutti, Fernando A. Osorio, Eric A. Nelson, Jane Christopher-Hennings, Tony L. Goldberg:
Ranking viruses: measures of positional importance within networks define core viruses for rational polyvalent vaccine development. 1624-1632 - Tim Rocktäschel, Michael Weidlich, Ulf Leser:
ChemSpot: a hybrid system for chemical named entity recognition. 1633-1640
- Clemens Kreutz, J. S. Gehring, Daniel Lang, Ralf Reski, Jens Timmer, Stefan A. Rensing:
TSSi - an R package for transcription start site identification from 5′ mRNA tag data. 1641-1642 - Vittore F. Scolari, Mina Zarei, Matteo Osella, Marco Cosentino Lagomarsino:
NuST: analysis of the interplay between nucleoid organization and gene expression. 1643-1644 - Joshua Tan, Durga Kuchibhatla, Fernanda L. Sirota, Westley A. Sherman, Tobias Gattermayer, Chia Yee Kwoh, Frank Eisenhaber, Georg Schneider, Sebastian Maurer-Stroh:
Tachyon search speeds up retrieval of similar sequences by several orders of magnitude. 1645-1646 - Matthew Kearse, Richard Moir, Amy Wilson, Steven Stones-Havas, Matthew Cheung, Shane S. Sturrock, Simon Buxton, Alex Cooper, Sidney Markowitz, Chris Duran, Tobias Thierer, Bruce Ashton, Peter L. Meintjes, Alexei J. Drummond:
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data. 1647-1649 - Weizhong Li, Hamish McWilliam, Mickael Goujon, Andrew Peter Cowley, Rodrigo Lopez, William R. Pearson:
PSI-Search: iterative HOE-reduced profile SSEARCH searching. 1650-1651 - Paulo C. Carvalho, John R. Yates III, Valmir Carneiro Barbosa:
Improving the TFold test for differential shotgun proteomics. 1652-1654 - Nicholas Smith, Shawn Witham, Subhra Sarkar, Jie Zhang, Lin Li, Chuan Li, Emil Alexov:
DelPhi web server v2: incorporating atomic-style geometrical figures into the computational protocol. 1655-1657 - Claudia Andreini, Gabriele Cavallaro, Serena Lorenzini:
FindGeo: a tool for determining metal coordination geometry. 1658-1660 - Adrià Cereto-Massagué, Laura Guasch, Cristina Valls, Miquel Mulero, Gerard Pujadas, Santiago Garcia-Vallvé:
DecoyFinder: an easy-to-use python GUI application for building target-specific decoy sets. 1661-1662 - Hadas Zur, Tamir Tuller:
RFMapp: ribosome flow model application. 1663-1664 - Marco Brandizi, Natalja Kurbatova, Ugis Sarkans, Philippe Rocca-Serra:
graph2tab, a library to convert experimental workflow graphs into tabular formats. 1665-1667
Volume 28, Number 13, July 2012
- Catherine A. Hayes, Szilárd Nemes, Niclas G. Karlsson:
Statistical analysis of glycosylation profiles to compare tissue type and inflammatory disease state. 1669-1676 - Shreepriya Das, Haris Vikalo:
OnlineCall: fast online parameter estimation and base calling for illumina's next-generation sequencing. 1677-1683
- Ari Löytynoja, Albert J. Vilella, Nick Goldman:
Accurate extension of multiple sequence alignments using a phylogeny-aware graph algorithm. 1684-1691 - Xiaowen Liu, Alessandro Mammana, Vineet Bafna:
Speeding up tandem mass spectral identification using indexes. 1692-1697 - Christian Otto, Peter F. Stadler, Steve Hoffmann:
Fast and sensitive mapping of bisulfite-treated sequencing data. 1698-1704
- Lars J. Kangas, Thomas O. Metz, Giorgis Isaac, Brian T. Schrom, Bojana Ginovska-Pangovska, Luning Wang, Li Tan, Robert R. Lewis, John H. Miller:
In silico identification software (ISIS): a machine learning approach to tandem mass spectral identification of lipids. 1705-1713
- Benedikt Zacher, Khalid Abnaof, Stephan Gade, Erfan Younesi, Achim Tresch, Holger Fröhlich:
Joint Bayesian inference of condition-specific miRNA and transcription factor activities from combined gene and microRNA expression data. 1714-1720 - Peter Glaus, Antti Honkela, Magnus Rattray:
Identifying differentially expressed transcripts from RNA-seq data with biological variation. 1721-1728
- Noah Zaitlen, Bogdan Pasaniuc, Nick Patterson, Samuela Pollack, Benjamin Voight, Leif Groop, David Altshuler, Brian E. Henderson, Laurence N. Kolonel, Loic Le Marchand, Kevin Waters, Christopher A. Haiman, Barbara E. Stranger, Emmanouil T. Dermitzakis, Peter Kraft, Alkes L. Price:
Analysis of case-control association studies with known risk variants. 1729-1737 - Benjamin A. Logsdon, Cara L. Carty, Alexander P. Reiner, James Y. Dai, Charles L. Kooperberg:
A novel variational Bayes multiple locus Z-statistic for genome-wide association studies with Bayesian model averaging. 1738-1744 - Dajiang J. Liu, Suzanne M. Leal:
SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations. 1745-1751
- Yu-Chieh Liao, Ming-Hsin Tsai, Feng-Chi Chen, Chao A. Hsiung:
GEMSiRV: a software platform for GEnome-scale metabolic model simulation, reconstruction and visualization. 1752-1758
- Makoto Miwa, Paul Thompson, Sophia Ananiadou:
Boosting automatic event extraction from the literature using domain adaptation and coreference resolution. 1759-1765 - Vân Anh Huynh-Thu, Yvan Saeys, Louis Wehenkel, Pierre Geurts:
Statistical interpretation of machine learning-based feature importance scores for biomarker discovery. 1766-1774 - Plamen Dragiev, Robert Nadon, Vladimir Makarenkov:
Two effective methods for correcting experimental high-throughput screening data. 1775-1782
- Robert Hoehndorf, Midori A. Harris, Heinrich Herre, Gabriella Rustici, Georgios V. Gkoutos:
Semantic integration of physiology phenotypes with an application to the Cellular Phenotype Ontology. 1783-1789
- Ji-Hong Kim, Hae-Jin Hu, Seon-Hee Yim, Joon Seol Bae, Seon-Young Kim, Yeun-Jun Chung:
CNVRuler: a copy number variation-based case-control association analysis tool. 1790-1792 - Maria Ortiz-Estevez, Ander Aramburu, Henrik Bengtsson, Pierre Neuvial, Angel Rubio:
CalMaTe: a method and software to improve allele-specific copy number of SNP arrays for downstream segmentation. 1793-1794
- Elena Yavorska Harris, Nadia Ponts, Karine G. Le Roch, Stefano Lonardi:
BRAT-BW: efficient and accurate mapping of bisulfite-treated reads. 1795-1796
- Phil H. Lee, Colm O'Dushlaine, Brett Thomas, Shaun Purcell:
INRICH: interval-based enrichment analysis for genome-wide association studies. 1797-1799
- Maria Anna Rapsomaniki, Panagiotis Kotsantis, Ioanna-Eleni Symeonidou, Nickolaos-Nikiforos Giakoumakis, Stavros L. Taraviras, Zoi Lygerou:
easyFRAP: an interactive, easy-to-use tool for qualitative and quantitative analysis of FRAP data. 1800-1801
- Noppadon Khiripet, Wongarnet Khantuwan, John R. Jungck:
Ka-me: a Voronoi image analyzer. 1802-1804
- Xiaoli Jiao, Brad T. Sherman, Da Wei Huang, Robert M. Stephens, Michael W. Baseler, H. Clifford Lane, Richard A. Lempicki:
DAVID-WS: a stateful web service to facilitate gene/protein list analysis. 1805-1806
Volume 28, Number 14, July 2012
- Terry Bertozzi, Kate L. Sanders, Mark J. Sistrom, Michael G. Gardner:
Anonymous nuclear loci in non-model organisms: making the most of high-throughput genome surveys. 1807-1810
- Christopher T. Saunders, Wendy S. W. Wong, Sajani Swamy, Jennifer Becq, Lisa J. Murray, R. Keira Cheetham:
Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairs. 1811-1817 - Arend Voorman, Ken Rice, Thomas Lumley:
Fast computation for genome-wide association studies using boosted one-step statistics. 1818-1822
- Elmar Pruesse, Jörg Peplies, Frank Oliver Glöckner:
SINA: Accurate high-throughput multiple sequence alignment of ribosomal RNA genes. 1823-1829 - Yongchao Liu, Bertil Schmidt, Douglas L. Maskell:
CUSHAW: a CUDA compatible short read aligner to large genomes based on the Burrows-Wheeler transform. 1830-1837 - Heng Li:
Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly. 1838-1844
- Joan Segura, Pamela F. Jones, Narcis Fernandez-Fuentes:
A holistic in silico approach to predict functional sites in protein structures. 1845-1850 - Maria T. Buenavista, Daniel B. Roche, Liam J. McGuffin:
Improvement of 3D protein models using multiple templates guided by single-template model quality assessment. 1851-1857 - David Hoksza, Daniel Svozil:
Efficient RNA pairwise structure comparison by SETTER method. 1858-1864
- Barbara Piasecka, Marc Robinson-Rechavi, Sven Bergmann:
Correcting for the bias due to expression specificity improves the estimation of constrained evolution of expression between mouse and human. 1865-1872 - Jishnu Das, Jaaved Mohammed, Haiyuan Yu:
Genome-scale analysis of interaction dynamics reveals organization of biological networks. 1873-1878
- Mingxiang Teng, Shoji Ichikawa, Leah R. Padgett, Yadong Wang, Matthew E. Mort, David N. Cooper, Daniel L. Koller, Tatiana Foroud, Howard J. Edenberg, Michael J. Econs, Yunlong Liu:
regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions. 1879-1886
- Daniela Beisser, Stefan Brunkhorst, Thomas Dandekar, Gunnar W. Klau, Marcus T. Dittrich, Tobias Müller:
Robustness and accuracy of functional modules in integrated network analysis. 1887-1894 - Doug Hyatt, Chongle Pan:
Exhaustive database searching for amino acid mutations in proteomes. 1895-1901 - Chen Zhao, Jianping Hua, Michael L. Bittner, Ivan Ivanov, Edward R. Dougherty:
Identifying mechanistic similarities in drug responses. 1902-1910
- Haisu Ma, Hongyu Zhao:
iFad: an integrative factor analysis model for drug-pathway association inference. 1911-1918
- Shane J. Neph, Scott Kuehn, Alex P. Reynolds, Eric Haugen, Robert E. Thurman, Audra K. Johnson, Eric Rynes, Matthew T. Maurano, Jeff Vierstra, Sean Thomas, Richard S. Sandstrom, Richard Humbert, John A. Stamatoyannopoulos:
BEDOPS: high-performance genomic feature operations. 1919-1920 - Pierre-Yves Chibon, Heiko Schoof, Richard G. F. Visser, Richard Finkers:
Marker2sequence, mine your QTL regions for candidate genes. 1921-1922
- Ken Chen, John W. Wallis, Cyriac Kandoth, Joelle M. Kalicki-Veizer, Karen L. Mungall, Andrew J. Mungall, Steven J. M. Jones, Marco A. Marra, Timothy J. Ley, Elaine R. Mardis, Richard K. Wilson, John N. Weinstein, Li Ding:
BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing data. 1923-1924 - Yuanwei Zhang, Bo Xu, Yifan Yang, Rongjun Ban, Huan Zhang, Xiaohua Jiang, Howard J. Cooke, Yu Xue, Qinghua Shi:
CPSS: a computational platform for the analysis of small RNA deep sequencing data. 1925-1927 - Nianxiang Zhang, Yan Xu, Martin O'Hely, Terence P. Speed, Curt Scharfe, Wenyi Wang:
SRMA: an R package for resequencing array data analysis. 1928-1930 - Marleen Claeys, Valerie Storms, Hong Sun, Tom Michoel, Kathleen Marchal:
MotifSuite: workflow for probabilistic motif detection and assessment. 1931-1932 - Jun Hu, Huanying Ge, Matthew Newman, Kejun Liu:
OSA: a fast and accurate alignment tool for RNA-Seq. 1933-1934 - Virag Sharma, David P. Murphy, Gregory M. Provan, Pavel V. Baranov:
CodonLogo: a sequence logo-based viewer for codon patterns. 1935-1936 - Thomas C. Conway, Jeremy Wazny, Andrew J. Bromage, Justin Zobel, Bryan Beresford-Smith:
Gossamer - a resource-efficient de novo assembler. 1937-1938
- John A. Dawson, Shuyun Ye, Christina Kendziorski:
R/EBcoexpress: an empirical Bayesian framework for discovering differential co-expression. 1939-1940 - Regis A. James, Mitchell M. Rao, Edward S. Chen, Margaret A. Goodell, Chad A. Shaw:
The Hematopoietic Expression Viewer: expanding mobile apps as a scientific tool. 1941-1942
- Chao Zhang, Kristina Hanspers, Allan Kuchinsky, Nathan Salomonis, Dong Xu, Alexander R. Pico:
Mosaic: making biological sense of complex networks. 1943-1944
- Arnaud Ogier, Thierry Dorval:
HCS-Analyzer: open source software for high-content screening data correction and analysis. 1945-1946
- Morgan G. I. Langille, Matthew R. Laird, William W. L. Hsiao, Terry A. Chiu, Jonathan A. Eisen, Fiona S. L. Brinkman:
MicrobeDB: a locally maintainable database of microbial genomic sequences. 1947-1948 - Shigeo Fujimori, Naoya Hirai, Kazuyo Masuoka, Tomohiro Oshikubo, Tatsuhiro Yamashita, Takanori Washio, Ayumu Saito, Masao Nagasaki, Satoru Miyano, Etsuko Miyamoto-Sato:
IRView: a database and viewer for protein interacting regions. 1949-1950
- David Ryan Koes, Carlos J. Camacho:
Small-molecule inhibitor starting points learned from protein-protein interaction inhibitor structure. 1951
Volume 28, Number 15, August 2012
- Luis Sánchez-Pulido, Lesheng Kong, Chris P. Ponting:
A common ancestry for BAP1 and Uch37 regulators. 1953-1956
- Attila Gyenesei, Jonathan Moody, Colin A. M. Semple, Chris S. Haley, Wenhua Wei:
High-throughput analysis of epistasis in genome-wide association studies with BiForce. 1957-1964 - Kai Fu, Qianzi Tang, Jianxing Feng, Xiaole Shirley Liu, Yong Zhang:
DiNuP: a systematic approach to identify regions of differential nucleosome positioning. 1965-1971
- Douglas L. Theobald, Phillip A. Steindel:
Optimal simultaneous superpositioning of multiple structures with missing data. 1972-1979 - Ernst Wit, David J. Bakewell:
Borrowing strength: a likelihood ratio test for related sparse signals. 1980-1989
- Jinghua Gu, Jianhua Xuan, Rebecca B. Riggins, Li Chen, Yue Joseph Wang, Robert Clarke:
Robust identification of transcriptional regulatory networks using a Gibbs sampler on outlier sum statistic. 1990-1997 - Carmen D. Tekwe, Raymond J. Carroll, Alan R. Dabney:
Application of survival analysis methodology to the quantitative analysis of LC-MS proteomics data. 1998-2003 - Moysés Nascimento, Thelma Sáfadi, Fabyano Fonseca e Silva, Ana Carolina C. Nascimento:
Bayesian model-based clustering of temporal gene expression using autoregressive panel data approach. 2004-2007
- Joshua S. Paul, Yun S. Song:
Blockwise HMM computation for large-scale population genomic inference. 2008-2015
- Martijn P. van Iersel, Alice Villéger, Tobias Czauderna, Sarah E. Boyd, Frank T. Bergmann, Augustin Luna, Emek Demir, Anatoly A. Sorokin, Ugur Dogrusöz, Yukiko Matsuoka, Akira Funahashi, Mirit I. Aladjem, Huaiyu Mi, Stuart L. Moodie, Hiroaki Kitano, Nicolas Le Novère, Falk Schreiber:
Software support for SBGN maps: SBGN-ML and LibSBGN. 2016-2021 - Yaki Setty:
Multi-scale computational modeling of developmental biology. 2022-2028 - Rami Mahdi, Abishek S. Madduri, Guoqing Wang, Yael Strulovici-Barel, Jacqueline Salit, Neil R. Hackett, Ronald G. Crystal, Jason G. Mezey:
Empirical Bayes conditional independence graphs for regulatory network recovery. 2029-2036 - Elad Noor, Arren Bar-Even, Avi I. Flamholz, Yaniv Lubling, Dan Davidi, Ron Milo:
An integrated open framework for thermodynamics of reactions that combines accuracy and coverage. 2037-2044 - Chihyun Park, Jaegyoon Ahn, Youngmi Yoon, Sanghyun Park:
Identification of functional CNV region networks using a CNV-gene mapping algorithm in a genome-wide scale. 2045-2051
- Yongchao Ge, Stuart C. Sealfon:
flowPeaks: a fast unsupervised clustering for flow cytometry data via K-means and density peak finding. 2052-2058
- Matthew B. Stocks, Simon Moxon, Daniel Mapleson, Hugh C. Woolfenden, Irina Mohorianu, Leighton Folkes, Frank Schwach, Tamas Dalmay, Vincent Moulton:
The UEA sRNA workbench: a suite of tools for analysing and visualizing next generation sequencing microRNA and small RNA datasets. 2059-2061 - Ashwini Jeggari, Debora S. Marks, Erik Larsson:
miRcode: a map of putative microRNA target sites in the long non-coding transcriptome. 2062-2063
- Alexandros Stamatakis, Andre J. Aberer, Christian Goll, Stephen A. Smith, Simon A. Berger, Fernando Izquierdo-Carrasco:
RAxML-Light: a tool for computing terabyte phylogenies. 2064-2066 - Vanderlei J. Debastiani, Valério D. Pillar:
SYNCSA - R tool for analysis of metacommunities based on functional traits and phylogeny of the community components. 2067-2068
- Rhonald C. Lua:
PyKnot: a PyMOL tool for the discovery and analysis of knots in proteins. 2069-2071 - Hannes Braberg, Benjamin M. Webb, Elina Tjioe, Ursula Pieper, Andrej Sali, Mallur S. Madhusudhan:
SALIGN: a web server for alignment of multiple protein sequences and structures. 2072-2073 - Andrea Volkamer, Daniel Kuhn, Friedrich Rippmann, Matthias Rarey:
DoGSiteScorer: a web server for automatic binding site prediction, analysis and druggability assessment. 2074-2075 - Masafumi Shionyu, Ken-ichi Takahashi, Mitiko Go:
AS-EAST: a functional annotation tool for putative proteins encoded by alternatively spliced transcripts. 2076-2077 - Srinivas Somarowthu, Mary Jo Ondrechen:
POOL server: machine learning application for functional site prediction in proteins. 2078-2079 - Tomás Di Domenico, Ian Walsh, Alberto J. M. Martin, Silvio C. E. Tosatto:
MobiDB: a comprehensive database of intrinsic protein disorder annotations. 2080-2081
- Olivier Sosnowski, Alain Charcosset, Johann Joets:
BioMercator V3: an upgrade of genetic map compilation and quantitative trait loci meta-analysis algorithms. 2082-2083 - Robert Kofler, Christian Schlötterer:
Gowinda: unbiased analysis of gene set enrichment for genome-wide association studies. 2084-2085 - Valentin Wimmer, Theresa Albrecht, Hans-Jürgen Auinger, Chris-Carolin Schön:
synbreed: a framework for the analysis of genomic prediction data using R. 2086-2087
- Jie Hao, William J. Astle, Maria De Iorio, Timothy M. D. Ebbels:
BATMAN - an R package for the automated quantification of metabolites from nuclear magnetic resonance spectra using a Bayesian model. 2088-2090
- David Osumi-Sutherland, Simon Reeve, Christopher J. Mungall, Fabian Neuhaus, Alan Ruttenberg, Gregory S. X. E. Jefferis, J. Douglas Armstrong:
A strategy for building neuroanatomy ontologies. 2091
Volume 28, Number 16, August 2012
- Vanessa E. Gray, Kimberly R. Kukurba, Sudhir Kumar:
Performance of computational tools in evaluating the functional impact of laboratory-induced amino acid mutations. 2093-2096
- Hayan Lee, Michael C. Schatz:
Genomic dark matter: the reliability of short read mapping illustrated by the genome mappability score. 2097-2105 - Jun Chen, Kyle Bittinger, Emily S. Charlson, Christian Hoffmann, James D. Lewis, Gary D. Wu, Ronald G. Collman, Frederic D. Bushman, Hongzhe Li:
Associating microbiome composition with environmental covariates using generalized UniFrac distances. 2106-2113
- Francesco Abate, Andrea Acquaviva, Giulia Paciello, Carmelo Foti, Elisa Ficarra, Alberto Ferrarini, Massimo Delledonne, Ilaria Iacobucci, Simona Soverini, Giovanni Martinelli, Enrico Macii:
Bellerophontes: an RNA-Seq data analysis framework for chimeric transcripts discovery based on accurate fusion model. 2114-2121 - Chandana Tennakoon, Rikky W. Purbojati, Wing-Kin Sung:
BatMis: a fast algorithm for k-mismatch mapping. 2122-2128
- Sayed Mohammad Ebrahim Sahraeian, Byung-Jun Yoon:
RESQUE: Network reduction using semi-Markov random walk scores for efficient querying of biological networks. 2129-2136 - Ömer Sinan Saraç, Vera Pancaldi, Jürg Bähler, Andreas Beyer:
Topology of functional networks predicts physical binding of proteins. 2137-2145 - Chao-Yi Dong, Dongkwan Shin, Sunghoon Joo, Yoonkey Nam, Kwang-Hyun Cho:
Identification of feedback loops in neural networks based on multi-step Granger causality. 2146-2153
- Martin Gerner, Farzaneh Sarafraz, Casey M. Bergman, Goran Nenadic:
BioContext: an integrated text mining system for large-scale extraction and contextualization of biomolecular events. 2154-2161 - Darby Tien-Hao Chang, Chao-Hsuan Ke, Jung-Hsin Lin, Jung-Hsien Chiang:
AutoBind: automatic extraction of protein-ligand-binding affinity data from biological literature. 2162-2168
- Robert Hoehndorf, Michel Dumontier, Georgios V. Gkoutos:
Identifying aberrant pathways through integrated analysis of knowledge in pharmacogenomics. 2169-2175
- Taemin Song, Kyu Baek Hwang, Michael Hsing, Kyungjoon Lee, Justin Bohn, Sek Won Kong:
gSearch: a fast and flexible general search tool for whole-genome sequencing. 2176-2177
- Lida Zhang, Yuyi Huang, Zehong Zou, Ying He, Ximo Chen, Ailin Tao:
SORTALLER: predicting allergens using substantially optimized algorithm on allergen family featured peptides. 2178-2179 - Zhifu Sun, Saurabh Baheti, Sumit Middha, Rahul Kanwar, Yuji Zhang, Xing Li, Andreas S. Beutler, Eric W. Klee, Yan W. Asmann, E. Aubrey Thompson, Jean-Pierre A. Kocher:
SAAP-RRBS: streamlined analysis and annotation pipeline for reduced representation bisulfite sequencing. 2180-2181 - Zejun Zheng, Stefan Kramer, Bertil Schmidt:
DySC: software for greedy clustering of 16S rRNA reads. 2182-2183 - Liguo Wang, Shengqin Wang, Wei Li:
RSeQC: quality control of RNA-seq experiments. 2184-2185
- Benjamin J. Bachman, Eric Venner, Rhonald C. Lua, Serkan Erdin, Olivier Lichtarge:
ETAscape: analyzing protein networks to predict enzymatic function and substrates in Cytoscape. 2186-2188 - Ian Walsh, Giovanni Minervini, Alessandra Corazza, Gennaro Esposito, Silvio C. E. Tosatto, Federico Fogolari:
Bluues server: electrostatic properties of wild-type and mutated protein structures. 2189-2190 - Ling-Hong Hung, Ram Samudrala:
Accelerated protein structure comparison using TM-score-GPU. 2191-2192 - Anna Caroline E. Dahl, Matthieu Chavent, Mark S. P. Sansom:
Bendix: intuitive helix geometry analysis and abstraction. 2193-2194
- Anat Kreimer, Adi Doron-Faigenboim, Elhanan Borenstein, Shiri Freilich:
NetCmpt: a network-based tool for calculating the metabolic competition between bacterial species. 2195-2197
- Wade K. Copeland, Vandhana Krishnan, Daniel Beck, Matt Settles, James A. Foster, Kyu-Chul Cho, Mitch Day, Roxana Hickey, Ursel M. E. Schütte, Xia Zhou, Christopher J. Williams, Larry J. Forney, Zaid Abdo:
mcaGUI: microbial community analysis R-Graphical User Interface (GUI). 2198-2199 - Jan Wildenhain, Nicholas FitzGerald, Mike Tyers:
MolClass: a web portal to interrogate diverse small molecule screen datasets with different computational models. 2200-2201 - Máté Szalay-Beko, Robin Palotai, Balázs Szappanos, István A. Kovács, Balázs Papp, Peter Csermely:
ModuLand plug-in for Cytoscape: determination of hierarchical layers of overlapping network modules and community centrality. 2202-2204
- Lihua Liu, Xi Ting Zhen, Emily Denton, Brian D. Marsden, Matthieu Schapira:
ChromoHub: a data hub for navigators of chromatin-mediated signalling. 2205-2206 - Javier Otegui, Arturo H. Ariño:
BIDDSAT: visualizing the content of biodiversity data publishers in the Global Biodiversity Information Facility network. 2207-2208 - Alexander C. Zambon, Stan Gaj, Isaac Ho, Kristina Hanspers, Karen Vranizan, Chris T. A. Evelo, Bruce R. Conklin, Alexander R. Pico, Nathan Salomonis:
GO-Elite: a flexible solution for pathway and ontology over-representation. 2209-2210
- Zengyou He, Haipeng Gong:
Comments on 'MMFPh: A Maximal Motif Finder for Phosphoproteomics Datasets'. 2211-2212 - Tuobin Wang, Arminja N. Kettenbach, Scott A. Gerber, Chris Bailey-Kellogg:
Response to 'Comments on "MMFPh: A Maximal Motif Finder for Phosphoproteomics Datasets"'. 2213
Volume 28, Number 17, September 2012
- Kristoffer Sahlin, Nathaniel Street, Joakim Lundeberg, Lars Arvestad:
Improved gap size estimation for scaffolding algorithms. 2215-2222 - Doug Hyatt, Philip F. LoCascio, Loren J. Hauser, Edward C. Uberbacher:
Gene and translation initiation site prediction in metagenomic sequences. 2223-2230
- Hiro Takahashi, Anna Takahashi, Satoshi Naito, Hitoshi Onouchi:
BAIUCAS: a novel BLAST-based algorithm for the identification of upstream open reading frames with conserved amino acid sequences and its application to the Arabidopsis thaliana genome. 2231-2241
- Gero Doose, Dirk Metzler:
Bayesian sampling of evolutionarily conserved RNA secondary structures with pseudoknots. 2242-2248 - Gwo-Yu Chuang, Jeffrey C. Boyington, M. Gordon Joyce, Jiang Zhu, Gary J. Nabel, Peter D. Kwong, Ivelin Georgiev:
Computational prediction of N-linked glycosylation incorporating structural properties and patterns. 2249-2255
- Tomas Puelma, Rodrigo A. Gutiérrez, Alvaro Soto:
Discriminative local subspaces in gene expression data for effective gene function prediction. 2256-2264
- Xiaoping Su, Li Zhang, Jianping Zhang, Funda Meric-Bernstam, John N. Weinstein:
PurityEst: estimating purity of human tumor samples using next-generation sequencing data. 2265-2266 - Lukas Habegger, Suganthi Balasubramanian, David Z. Chen, Ekta Khurana, Andrea Sboner, Arif Ozgun Harmanci, Joel S. Rozowsky, Declan Clarke, Michael Snyder, Mark Gerstein:
VAT: a computational framework to functionally annotate variants in personal genomes within a cloud-computing environment. 2267-2269 - Sebastian Gibb, Korbinian Strimmer:
MALDIquant: a versatile R package for the analysis of mass spectrometry data. 2270-2271
- Anton Zoubarev, Kelsey M. Hamer, Kiran Keshav, E. Luke McCarthy, Joseph Roy C. Santos, Thea Van Rossum, Cameron McDonald, Adam Hall, Xiang Wan, Raymond Lim, Jesse A. Gillis, Paul Pavlidis:
Gemma: a resource for the reuse, sharing and meta-analysis of expression profiling data. 2272-2273
- Nikolaos Alachiotis, Alexandros Stamatakis, Pavlos Pavlidis:
OmegaPlus: a scalable tool for rapid detection of selective sweeps in whole-genome datasets. 2274-2275
- Johannes Klein, Stefan Leupold, Ilona Biegler, Rebekka Biedendieck, Richard Münch, Dieter Jahn:
TLM-Tracker: software for cell segmentation, tracking and lineage analysis in time-lapse microscopy movies. 2276-2277 - Florence Nicolè, Yann Guitton, Elodie A. Courtois, Sandrine Moja, Laurent Legendre, Martine Hossaert-McKey:
MSeasy: unsupervised and untargeted GC-MS data processing. 2278-2280 - Rodrigo Santamaría, Philippe Pierre:
Voronto: mapper for expression data to ontologies. 2281-2282 - Peter M. Krempl, Jürgen Mairhofer, Gerald Striedner, Gerhard G. Thallinger:
A sequence comparison and gene expression data integration add-on for the Pathway Tools software. 2283-2284
- David Salgado, Martin Krallinger, Marc Depaule, Elodie Drula, Ashish V. Tendulkar, Florian Leitner, Alfonso Valencia, Christophe Marcelle:
MyMiner: a web application for computer-assisted biocuration and text annotation. 2285-2287 - Dmitry Grapov, John W. Newman:
imDEV: a graphical user interface to R multivariate analysis tools in Microsoft Excel. 2288-2290
- Liming Lai, Arthur Liberzon, Jason Hennessey, Gaixin Jiang, Jianli Qi, Jill P. Mesirov, Steven X. Ge:
AraPath: a knowledgebase for pathway analysis in Arabidopsis. 2291-2292 - Tzong-Yi Lee, Yi-Ju Chen, Cheng-Tsung Lu, Wei-Chieh Ching, Yu-Chuan Teng, Hsien-Da Huang, Yu-Ju Chen:
dbSNO: a database of cysteine S-nitrosylation. 2293-2295
Volume 28, Number 18, September 2012
- Torsten Schwede, Dagmar Iber:
ECCB 2012: The 11th European Conference on Computational Biology. 303-305 - Ma'ayan Bresler, Sara Sheehan, Andrew H. Chan, Yun S. Song:
Telescoper: de novo assembly of highly repetitive regions. 311-317 - Yongchao Liu, Bertil Schmidt:
Long read alignment based on maximal exact match seeds. 318-324 - Md Pavel Mahmud, John Wiedenhoeft, Alexander Schliep:
Indel-tolerant read mapping with trinucleotide frequencies using cache-oblivious kd-trees. 325-332 - Tobias Rausch, Thomas Zichner, Andreas Schlattl, Adrian M. Stütz, Vladimir Benes, Jan O. Korbel:
DELLY: structural variant discovery by integrated paired-end and split-read analysis. 333-339 - Alexander C. J. Roth:
Decoding properties of tRNA leave a detectable signal in codon usage bias. 340-348 - Matthew Ruffalo, Mehmet Koyutürk, Soumya Ray, Thomas LaFramboise:
Accurate estimation of short read mapping quality for next-generation genome sequencing. 349-355 - Yi Wang, Henry C. M. Leung, Siu-Ming Yiu, Francis Y. L. Chin:
MetaCluster 5.0: a two-round binning approach for metagenomic data for low-abundance species in a noisy sample. 356-362 - Yu-Wei Wu, Mina Rho, Thomas G. Doak, Yuzhen Ye:
Stitching gene fragments with a network matching algorithm improves gene assembly for metagenomics. 363-369
- Lachlan James M. Coin, Dandan Cao, Jingjing Ren, Xianbo Zuo, Liangdan Sun, Sen Yang, Xuejun Zhang, Yong Cui, Yingrui Li, Xin Jin, Jun Wang:
An exome sequencing pipeline for identifying and genotyping common CNVs associated with disease with application to psoriasis. 370-374 - Hongjie Zhu, Lexin Li, Hua Zhou:
Nonlinear dimension reduction with Wright-Fisher kernel for genotype aggregation and association mapping. 375-381
- Sèverine Bérard, Coralie Gallien, Bastien Boussau, Gergely J. Szöllosi, Vincent Daubin, Eric Tannier:
Evolution of gene neighborhoods within reconciled phylogenies. 382-388 - Ofir Cohen, Haim Ashkenazy, David Burstein, Tal Pupko:
Uncovering the co-evolutionary network among prokaryotic genes. 389-394 - Slavica Dimitrieva, Philipp Bucher:
Genomic context analysis reveals dense interaction network between vertebrate ultraconserved non-coding elements. 395-401 - David Sankoff, Chunfang Zheng:
Fractionation, rearrangement and subgenome dominance. 402-408 - Maureen Stolzer, Han Lai, Minli Xu, Deepa Sathaye, Benjamin Vernot, Dannie Durand:
Inferring duplications, losses, transfers and incomplete lineage sorting with nonbinary species trees. 409-415
- Fayyaz ul Amir Afsar Minhas, Asa Ben-Hur:
Multiple instance learning of Calmodulin binding sites. 416-422 - Francis Gaudreault, Matthieu Chartier, Rafael Najmanovich:
Side-chain rotamer changes upon ligand binding: common, crucial, correlate with entropy and rearrange hydrogen bonding. 423-430 - Morten Källberg, Nitin Bhardwaj, Robert E. Langlois, Hui Lu:
A structure-based protocol for learning the family-specific mechanisms of membrane-binding domains. 431-437 - Patrik Koskinen, Liisa Holm:
SANS: high-throughput retrieval of protein sequences allowing 50% mismatches. 438-443 - Mario Abdel Messih, Meghana Chitale, Vladimir B. Bajic, Daisuke Kihara, Xin Gao:
Protein domain recurrence and order can enhance prediction of protein functions. 444-450
- Enrico Glaab, Anaïs Baudot, Natalio Krasnogor, Reinhard Schneider, Alfonso Valencia:
EnrichNet: network-based gene set enrichment analysis. 451-457 - Tatyana Goldberg, Tobias Hamp, Burkhard Rost:
LocTree2 predicts localization for all domains of life. 458-465 - Meghana Kshirsagar, Jaime G. Carbonell, Judith Klein-Seetharaman:
Techniques to cope with missing data in host-pathogen protein interaction prediction. 466-472 - Yu-Keng Shih, Srinivasan Parthasarathy:
Identifying functional modules in interaction networks through overlapping Markov clustering. 473-479 - Ryan W. Solava, Ryan P. Michaels, Tijana Milenkovic:
Graphlet-based edge clustering reveals pathogen-interacting proteins. 480-486 - Yasuo Tabei, Edouard Pauwels, Véronique Stoven, Kazuhiro Takemoto, Yoshihiro Yamanishi:
Identification of chemogenomic features from drug-target interaction networks using interpretable classifiers. 487-494
- Amit Singh, Juliana M. Nascimento, Silke Kowar, Hauke Busch, Melanie Boerries:
Boolean approach to signalling pathway modelling in HGF-induced keratinocyte migration. 495-501 - Abdelhalim Larhlimi, Georg Basler, Sergio Grimbs, Joachim Selbig, Zoran Nikoloski:
Stoichiometric capacitance reveals the theoretical capabilities of metabolic networks. 502-508 - Jie Li, Xu Hua, Martin Haubrock, Jin Wang, Edgar Wingender:
The architecture of the gene regulatory networks of different tissues. 509-514 - Daniel Machado, Zita Soons, Kiran Raosaheb Patil, Eugénio C. Ferreira, Isabel Rocha:
Random sampling of elementary flux modes in large-scale metabolic networks. 515-521 - Sayaka Mizutani, Edouard Pauwels, Véronique Stoven, Susumu Goto, Yoshihiro Yamanishi:
Relating drug-protein interaction network with drug side effects. 522-528 - Max Schelker, Andreas Raue, Jens Timmer, Clemens Kreutz:
Comprehensive estimation of input signals and dynamics in biochemical reaction networks. 529-534 - Patrick Weber, Andrei Kramer, Clemens Dingler, Nicole Radde:
Trajectory-oriented Bayesian experiment design versus Fisher A-optimal design: an in depth comparison study. 535-541
- Günter Jäger, Florian Battke, Kay Nieselt:
Reveal - visual eQTL analytics. 542-548 - Michael Klann, Arnab Ganguly, Heinz Koeppl:
Hybrid spatial Gillespie and particle tracking simulation. 549-555 - Nico Scherf, Maria Herberg, Konstantin Thierbach, Thomas Zerjatke, Tuzer Kalkan, Peter Humphreys, Austin Smith, Ingmar Glauche, Ingo Roeder:
Imaging, quantification and visualization of spatio-temporal patterning in mESC colonies under different culture conditions. 556-561
- Michael J. Bell, Colin S. Gillespie, Daniel Swan, Phillip W. Lord:
An approach to describing and analysing bulk biological annotation quality: a case study using UniProtKB. 562-568 - Ernesto Iacucci, Léon-Charles Tranchevent, Dusan Popovic, Georgios A. Pavlopoulos, Bart De Moor, Reinhard Schneider, Yves Moreau:
ReLiance: a machine learning and literature-based prioritization of receptor - ligand pairings. 569-574 - Sampo Pyysalo, Tomoko Ohta, Makoto Miwa, Han-Cheol Cho, Junichi Tsujii, Sophia Ananiadou:
Event extraction across multiple levels of biological organization. 575-581
- Seungyeoun Lee, Min-Seok Kwon, Jung Mi Oh, Taesung Park:
Gene-gene interaction analysis for the survival phenotype based on the Cox model. 582-588 - Nico Pfeifer, Thomas Lengauer:
Improving HIV coreceptor usage prediction in the clinic using hints from next-generation sequencing data. 589-595 - Thang V. Pham, Connie R. Jimenez:
An accurate paired sample test for count data. 596-602 - Peter Sykacek:
Bayesian assignment of gene ontology terms to gene expression experiments. 603-610 - Masataka Takarabe, Masaaki Kotera, Yosuke Nishimura, Susumu Goto, Yoshihiro Yamanishi:
Drug target prediction using adverse event report systems: a pharmacogenomic approach. 611-618 - Hua Wang, Feiping Nie, Heng Huang, Jingwen Yan, Sungeun Kim, Kwangsik Nho, Shannon L. Risacher, Andrew J. Saykin, Li Shen:
From phenotype to genotype: an association study of longitudinal phenotypic markers to Alzheimer's disease relevant SNPs. 619-625
- Florian Buettner, Fabian J. Theis:
A novel approach for resolving differences in single-cell gene expression patterns from zygote to blastocyst. 626-632 - Hiroshi Hatsuda:
Finding differentially expressed regions of arbitrary length in quantitative genomic data based on marked point process model. 633-639 - Sam Ng, Eric A. Collisson, Artem Sokolov, Theodore Goldstein, Abel Gonzalez-Perez, Núria López-Bigas, Christopher Benz, David Haussler, Joshua M. Stuart:
PARADIGM-SHIFT predicts the function of mutations in multiple cancers using pathway impact analysis. 640-646
- Thaís Gaudencio do Rêgo, Helge G. Roider, Francisco de A. T. de Carvalho, Ivan G. Costa:
Inferring epigenetic and transcriptional regulation during blood cell development with a mixture of sparse linear models. 2297-2303
- Mehmet Gönen:
Predicting drug-target interactions from chemical and genomic kernels using Bayesian matrix factorization. 2304-2310 - Federica Eduati, Javier De Las Rivas, Barbara Di Camillo, Gianna Toffolo, Julio Saez-Rodriguez:
Integrating literature-constrained and data-driven inference of signalling networks. 2311-2317 - Thomas Sakoparnig, Niko Beerenwinkel:
Efficient sampling for Bayesian inference of conjunctive Bayesian networks. 2318-2324 - Jianlong Qi, Tom Michoel:
Context-specific transcriptional regulatory network inference from global gene expression maps using double two-way t-tests. 2325-2332 - Markus Heinonen, Huibin Shen, Nicola Zamboni, Juho Rousu:
Metabolite identification and molecular fingerprint prediction through machine learning. 2333-2341 - Chris J. Oates, Bryan T. J. Hennessy, Yiling Lu, Gordon B. Mills, Sach Mukherjee:
Network inference using steady-state data and Goldbeter-koshland kinetics. 2342-2348
- Elisabeth Georgii, Jarkko Salojärvi, Mikael Brosché, Jaakko Kangasjärvi, Samuel Kaski:
Targeted retrieval of gene expression measurements using regulatory models. 2349-2356
- Guillem Rigaill, Sidney Cadot, Roelof J. C. Kluin, Zheng Xue, René Bernards, Ian J. Majewski, Lodewyk F. A. Wessels:
A regression model for estimating DNA copy number applied to capture sequencing data. 2357-2365
- John C. Mu, Hui Jiang, Amirhossein Kiani, Marghoob Mohiyuddin, Narges Bani Asadi, Wing Hung Wong:
Fast and accurate read alignment for resequencing. 2366-2373
- Boguslaw Obara, Vicente Grau, Mark D. Fricker:
A bioimage informatics approach to automatically extract complex fungal networks. 2374-2381
- Pei Li, Guoli Ji, Min Dong, Emily Schmidt, Douglas Lenox, Liangliang Chen, Qi Liu, Lin Liu, Jie Zhang, Chun Liang:
CBrowse: a SAM/BAM-based contig browser for transcriptome assembly visualization and analysis. 2382-2384 - Michael C. Ryan, James A. Cleland, RyangGuk Kim, Wing Chung Wong, John N. Weinstein:
SpliceSeq: a resource for analysis and visualization of RNA-Seq data on alternative splicing and its functional impacts. 2385-2387
- Bradley R. Jones, Ashok Rajaraman, Eric Tannier, Cédric Chauve:
ANGES: reconstructing ANcestral GEnomeS maps. 2388-2390
- Arun Prasad Pandurangan, Maya Topf:
RIBFIND: a web server for identifying rigid bodies in protein structures and to aid flexible fitting into cryo EM maps. 2391-2393 - Carles Pons, Daniel Jiménez-González, Cecilia González-Alvarez, Harald Servat, Daniel Cabrera-Benitez, Xavier Aguilar, Juan Fernández-Recio:
Cell-Dock: high-performance protein-protein docking. 2394-2396
- Alexander E. Lipka, Feng Tian, Qishan Wang, Jason Peiffer, Meng Li, Peter J. Bradbury, Michael A. Gore, Edward S. Buckler, Zhiwu Zhang:
GAPIT: genome association and prediction integrated tool. 2397-2399
- Michael D. Linderman, Zach Bjornson, Erin F. Simonds, Peng Qiu, Robert V. Bruggner, Ketaki Sheode, Teresa H. Meng, Sylvia K. Plevritis, Garry P. Nolan:
CytoSPADE: high-performance analysis and visualization of high-dimensional cytometry data. 2400-2401 - Matthias König, Andreas Dräger, Hermann-Georg Holzhütter:
CySBML: a Cytoscape plugin for SBML. 2402-2403
- Thomas Taverner, Yuliya V. Karpievitch, Ashoka D. Polpitiya, Joseph N. Brown, Alan R. Dabney, Gordon A. Anderson, Richard D. Smith:
DanteR: an extensible R-based tool for quantitative analysis of -omics data. 2404-2406
Volume 28, Number 19, October 2012
- Dapeng Zhang, Lakshminarayan M. Iyer, L. Aravind:
Bacterial GRAS domain proteins throw new light on gibberellic acid response mechanisms. 2407-2411
- Toshiro K. Ohsumi, Mark L. Borowsky:
MolBioLib: a C++11 framework for rapid development and deployment of bioinformatics tasks. 2412-2416
- Gregory G. Faust, Ira M. Hall:
YAHA: fast and flexible long-read alignment with optimal breakpoint detection. 2417-2424 - Thomas C. Freeman Jr., William C. Wimley:
TMBB-DB: a transmembrane β-barrel proteome database. 2425-2430
- Edvin Fuglebakk, Julian Echave, Nathalie Reuter:
Measuring and comparing structural fluctuation patterns in large protein datasets. 2431-2440 - Jaume Bacardit, Pawel Widera, Alfonso E. Márquez Chamorro, Federico Divina, Jesús S. Aguilar-Ruiz, Natalio Krasnogor:
Contact map prediction using a large-scale ensemble of rule sets and the fusion of multiple predicted structural features. 2441-2448 - Pietro di Lena, Ken Nagata, Pierre Baldi:
Deep architectures for protein contact map prediction. 2449-2457
- Wenyuan Li, Shi-Hua Zhang, Chun-Chi Liu, Xianghong Jasmine Zhou:
Identifying multi-layer gene regulatory modules from multi-dimensional genomic data. 2458-2466
- Z. Zhang, François Guillaume, A. Sartelet, Carole Charlier, Michel Georges, Frédéric Farnir, Tom Druet:
Ancestral haplotype-based association mapping with generalized linear mixed models accounting for stratification. 2467-2473
- Vicente Acuña, Paulo Vieira Milreu, Ludovic Cottret, Alberto Marchetti-Spaccamela, Leen Stougie, Marie-France Sagot:
Algorithms and complexity of enumerating minimal precursor sets in genome-wide metabolic networks. 2474-2483 - Daniel Gusenleitner, Eleanor Howe, Stefan Bentink, John Quackenbush, Aedín C. Culhane:
iBBiG: iterative binary bi-clustering of gene sets. 2484-2492 - Xiaoquan Su, Jian Xu, Kang Ning:
Meta-Storms: efficient search for similar microbial communities based on a novel indexing scheme and similarity score for metagenomic data. 2493-2501
- Sebastian Bauer, Sebastian Köhler, Marcel H. Schulz, Peter N. Robinson:
Bayesian ontology querying for accurate and noise-tolerant semantic searches. 2502-2508
- Rolf Hilker, Corinna Sickinger, Christian N. S. Pedersen, Jens Stoye:
UniMoG - a unifying framework for genomic distance calculation and sorting based on DCJ. 2509-2511 - Sandro Morganella, Michele Ceccarelli:
VegaMC: a R/bioconductor package for fast downstream analysis of large array comparative genomic hybridization datasets. 2512-2514 - Tom Kamphans, Peter M. Krawitz:
GeneTalk: an expert exchange platform for assessing rare sequence variants in personal genomes. 2515-2516 - Valentina Boeva, Alban Lermine, Camille Barette, Christel Guillouf, Emmanuel Barillot:
Nebula - a web-server for advanced ChIP-seq data analysis. 2517-2519 - Johannes Köster, Sven Rahmann:
Snakemake - a scalable bioinformatics workflow engine. 2520-2522
- Peter Menzel, Stefan E. Seemann, Jan Gorodkin:
RILogo: visualizing RNA-RNA interactions. 2523-2526 - Monzoorul Haque Mohammed, Anirban Dutta, Tungadri Bose, Sudha Chadaram, Sharmila S. Mande:
DELIMINATE - a fast and efficient method for loss-less compression of genomic sequences: Sequence analysis. 2527-2529
- Ronny Lorenz, Ivo L. Hofacker, Stephan H. Bernhart:
Folding RNA/DNA hybrid duplexes. 2530-2531
- Nicolas Delhomme, Ismaël Padioleau, Eileen E. M. Furlong, Lars M. Steinmetz:
easyRNASeq: a bioconductor package for processing RNA-Seq data. 2532-2533 - Xingbin Wang, Dongwan D. Kang, Kui Shen, Chi Song, Shuya Lu, Lun-Ching Chang, Serena G. Liao, Zhiguang Huo, Shaowu Tang, Ying Ding, Naftali Kaminski, Etienne Sibille, Yan Lin, Jia Li, George C. Tseng:
An R package suite for microarray meta-analysis in quality control, differentially expressed gene analysis and pathway enrichment detection. 2534-2536
- Rod Peakall, Peter E. Smouse:
GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research - an update. 2537-2539 - Sang Hong Lee, Jian Yang, M. E. Goddard, Peter M. Visscher, Naomi R. Wray:
Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. 2540-2542 - Jacqueline I. Goldstein, Andrew Crenshaw, Jason P. Carey, George B. Grant, Jared Maguire, Menachem Fromer, Colm O'Dushlaine, Jennifer L. Moran, Kimberly Chambert, Christine Stevens, Pamela Sklar, Christina M. Hultman, Shaun Purcell, Steven A. McCarroll, Patrick F. Sullivan, Mark J. Daly, Benjamin M. Neale:
zCall: a rare variant caller for array-based genotyping: Genetics and population analysis. 2543-2545
- Dorothee Girbig, Joachim Selbig, Sergio Grimbs:
A MATLAB toolbox for structural kinetic modeling. 2546-2547
- Wenzhou Li, Heather A. O'Neill, Vicki H. Wysocki:
SQID-XLink: implementation of an intensity-incorporated algorithm for cross-linked peptide identification. 2548-2550
- Ming-an Sun, Yejun Wang, Han Cheng, Qing Zhang, Wei Ge, Dianjing Guo:
RedoxDB - a curated database for experimentally verified protein oxidative modification. 2551-2552 - Sonu Kumar, Thomas Lütteke, Reinhard Schwartz-Albiez:
GlycoCD: a repository for carbohydrate-related CD antigens. 2553-2555
- Burkhard Rost, Terry Gaasterland, Thomas Lengauer, Michal Linial, Scott Markel, B. J. Morrison McKay, Reinhard Schneider, Paul Horton, Janet Kelso:
Paving the future: finding suitable ISMB venues. 2556-2559
- Anat Kreimer, Adi Doron-Faigenboim, Elhanan Borenstein, Shiri Freilich:
NetCmpt: a network-based tool for calculating the metabolic competition between bacterial species. 2560
Volume 28, Number 20, October 2012
- Changqing Zhang, Guangping Li, Jin Wang, Jinggui Fang:
Identification of trans-acting siRNAs and their regulatory cascades in grapevine. 2561-2568 - Baiyu Zhou:
An empirical Bayes mixture model for SNP detection in pooled sequencing data. 2569-2575
- Yue Jiang, Yadong Wang, Michael Brudno:
PRISM: Pair-read informed split-read mapping for base-pair level detection of insertion, deletion and structural variants. 2576-2583 - Zhaonan Sun, Yu Zhu:
Systematic comparison of RNA-Seq normalization methods using measurement error models. 2584-2591 - David Weese, Manuel Holtgrewe, Knut Reinert:
RazerS 3: Faster, fully sensitive read mapping. 2592-2599
- Iain H. Moal, Juan Fernández-Recio:
SKEMPI: a Structural Kinetic and Energetic database of Mutant Protein Interactions and its use in empirical models. 2600-2607 - Ryan Brenke, David R. Hall, Gwo-Yu Chuang, Stephen R. Comeau, Tanggis Bohnuud, Dmitri Beglov, Ora Schueler-Furman, Sandor Vajda, Dima Kozakov:
Application of asymmetric statistical potentials to antibody-protein docking. 2608-2614
- Raymond Walters, Charles Laurin, Gitta H. Lubke:
An integrated approach to reduce the impact of minor allele frequency and linkage disequilibrium on variable importance measures for genome-wide data. 2615-2623
- Boon-Siew Seah, Sourav S. Bhowmick, C. Forbes Dewey Jr.:
FACETS: multi-faceted functional decomposition of protein interaction networks. 2624-2631 - Ernest Lo, Emmanuelle Soleilhac, Anne Martinez, Laurence Lafanechère, Robert Nadon:
Intensity quantile estimation and mapping - a novel algorithm for the correction of image non-uniformity bias in HCS data. 2632-2639 - Peng Yang, Xiaoli Li, Jian-Ping Mei, Chee Keong Kwoh, See-Kiong Ng:
Positive-unlabeled learning for disease gene identification. 2640-2647 - Finja Büchel, Clemens Wrzodek, Florian Mittag, Andreas Dräger, Johannes Eichner, Nicolas Rodriguez, Nicolas Le Novère, Andreas Zell:
Qualitative translation of relations from BioPAX to SBML qual. 2648-2653
- Quoc-Chinh Bui, Peter M. A. Sloot:
A robust approach to extract biomedical events from literature. 2654-2661 - Haisu Ma, Hongyu Zhao:
FacPad: Bayesian sparse factor modeling for the inference of pathways responsive to drug treatment. 2662-2670
- Anika Groß, Michael Hartung, Kay Prüfer, Janet Kelso, Erhard Rahm:
Impact of ontology evolution on functional analyses. 2671-2677
- Fernando García-Alcalde, Konstantin Okonechnikov, José Carbonell, Luis M. Cruz, Stefan Götz, Sonia Tarazona, Joaquín Dopazo, Thomas F. Meyer, Ana Conesa:
Qualimap: evaluating next-generation sequencing alignment data. 2678-2679
- Valerie Hower, Richard Starfield, Adam Roberts, Lior Pachter:
Quantifying uniformity of mapped reads. 2680-2682 - Paulo Gaspar, José Luís Oliveira, Jörg Frommlet, Manuel A. S. Santos, Gabriela R. Moura:
EuGene: maximizing synthetic gene design for heterologous expression. 2683-2684 - Sudhir Kumar, Glen Stecher, Daniel Peterson, Koichiro Tamura:
MEGA-CC: computing core of molecular evolutionary genetics analysis program for automated and iterative data analysis. 2685-2686 - Narendra Kumar, Jeffrey Skolnick:
EFICAz2.5: application of a high-precision enzyme function predictor to 396 proteomes. 2687-2688
- Stephen A. Smith, Brian C. O'Meara:
treePL: divergence time estimation using penalized likelihood for large phylogenies. 2689-2690
- Zsuzsanna Sükösd, Bjarne Knudsen, Jørgen Kjems, Christian N. S. Pedersen:
PPfold 3.0: fast RNA secondary structure prediction using phylogeny and auxiliary data. 2691-2692 - Andreas Prlic, Andrew D. Yates, Spencer Bliven, Peter W. Rose, Julius O. B. Jacobsen, Peter V. Troshin, Mark Chapman, Jianjiong Gao, Chuan Hock Koh, Sylvain Foisy, Richard C. G. Holland, Gediminas Rimsa, Michael L. Heuer, Hannes Brandstätter-Müller, Philip E. Bourne, Scooter Willis:
BioJava: an open-source framework for bioinformatics in 2012. 2693-2695 - Dong Zhang, Xingran Xue, Russell L. Malmberg, Liming Cai:
TRFolder-W: a web server for telomerase RNA structure prediction in yeast genomes. 2696-2697
- Vikas Gupta, Katharina Markmann, Christian N. S. Pedersen, Jens Stougaard, Stig U. Andersen:
shortran: a pipeline for small RNA-seq data analysis. 2698-2700 - Roberto-Rafael Ramos-Rodriguez, Raquel Cuevas-Diaz-Duran, Francesco Falciani, José Gerardo Tamez-Peña, Victor Trevino:
COMPADRE: an R and web resource for pathway activity analysis by component decompositions. 2701-2702
- Biao Li, Gao T. Wang, Suzanne M. Leal:
SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits. 2703-2704
- Leslie Aïchaoui, Matthieu Jules, Ludovic Le Chat, Stéphane Aymerich, Vincent Fromion, Anne Goelzer:
BasyLiCA: a tool for automatic processing of a Bacterial Live Cell Array. 2705-2706
- Miguel Rojas-Chertó, Michael van Vliet, Julio E. Peironcely, Ronnie van Doorn, Maarten Kooyman, Tim te Beek, Marc A. van Driel, Thomas Hankemeier, Theo H. Reijmers:
MetiTree: a web application to organize and process high-resolution multi-stage mass spectrometry metabolomics data. 2707-2709
Volume 28, Number 21, November 2012
- Teo Shu Mei, Yudi Pawitan, Ku Chee Seng, Kee Seng Chia, Agus Salim:
Statistical challenges associated with detecting copy number variations with next-generation sequencing. 2711-2718
- Zhiming Dai, Xianhua Dai:
Antisense transcription is coupled to nucleosome occupancy in sense promoters. 2719-2723
- Trevor Paterson, Andy Law:
JEnsembl: a version-aware Java API to Ensembl data systems. 2724-2731
- Zechen Chong, Jue Ruan, Chung-I Wu:
Rainbow: an integrated tool for efficient clustering and assembling RAD-seq reads. 2732-2737 - Anne Wenzel, Erdinç Akbasli, Jan Gorodkin:
RIsearch: fast RNA-RNA interaction search using a simplified nearest-neighbor energy model. 2738-2746 - Vincent Plagnol, James Curtis, Michael Epstein, Kin Y. Mok, Emma Stebbings, Sofia Grigoriadou, Nicholas W. Wood, Sophie Hambleton, Siobhan O. Burns, Adrian J. Thrasher, Dinakantha Kumararatne, Rainer Doffinger, Sergey Nejentsev:
A robust model for read count data in exome sequencing experiments and implications for copy number variant calling. 2747-2754
- Juliana R. Rocha, Marx G. van der Linden, Diogo C. Ferreira, Paulo H. Azevêdo, Antônio F. Pereira de Araújo:
Information-theoretic analysis and prediction of protein atomic burials: on the search for an informational intermediate between sequence and structure. 2755-2762 - Qifang Xu, Roland L. Dunbrack Jr.:
Assignment of protein sequences to existing domain and family classification systems: Pfam and the PDB. 2763-2772
- Bruce A. Rosa, Ji Zhang, Ian T. Major, Wensheng Qin, Jin Chen:
Optimal timepoint sampling in high-throughput gene expression experiments. 2773-2781 - Jianxing Feng, Clifford A. Meyer, Qian Wang, Jun S. Liu, Xiaole Shirley Liu, Yong Zhang:
GFOLD: a generalized fold change for ranking differentially expressed genes from RNA-seq data. 2782-2788 - Robert C. McLeay, Tom Lesluyes, Gabriel Cuéllar-Partida, Timothy L. Bailey:
Genome-wide in silico prediction of gene expression. 2789-2796
- Alexander G. Churbanov, Rachael Ryan, Nabeeh Hasan, Donovan Bailey, Haofeng Chen, Brook Milligan, Peter Houde:
HighSSR: high-throughput SSR characterization and locus development from next-gen sequencing data. 2797-2803
- Steven M. Hill, Yiling Lu, Jennifer Molina, Laura Heiser, Paul T. Spellman, Terence P. Speed, Joe W. Gray, Gordon B. Mills, Sach Mukherjee:
Bayesian Inference of Signaling Network Topology in a Cancer Cell Line. 2804-2810 - Ariel Feiglin, Adar Hacohen, Avital Sarusi, Jasmin Fisher, Ron Unger, Yanay Ofran:
Static network structure can be used to model the phenotypic effects of perturbations in regulatory networks. 2811-2818 - Daniel J. Stekhoven, Izabel Moraes, Gardar Sveinbjörnsson, Lars Hennig, Marloes H. Maathuis, Peter Bühlmann:
Causal stability ranking. 2819-2823
- Mohammadmahdi R. Yousefi, Edward R. Dougherty:
Performance reproducibility index for classification. 2824-2833 - Haitian Wang, Shaw-Hwa Lo, Tian Zheng, Inchi Hu:
Interaction-based feature selection and classification for high-dimensional biological data. 2834-2842
- Nicolas Servant, Bryan R. Lajoie, Elphège P. Nora, Luca Giorgetti, Chong-Jian Chen, Edith Heard, Job Dekker, Emmanuel Barillot:
HiTC: exploration of high-throughput 'C' experiments. 2843-2844 - Alan E. Barber II, Patricia C. Babbitt:
Pythoscape: a framework for generation of large protein similarity networks. 2845-2846
- Sudhir Kumar, Kelly Boccia, Michael McCutchan, Jieping Ye:
Exploring spatial patterns of gene expression from Fruit Fly embryogenesis on the iPhone. 2847-2848
- Yoshitsugu Konishi, Kiyoko F. Aoki-Kinoshita:
The GlycomeAtlas tool for visualizing and querying glycome data. 2849-2850
- Tiejun Cheng, Yanli Wang, Stephen H. Bryant:
FSelector: a Ruby gem for feature selection. 2851-2852
- Ratheesh Kumar R., Nagarajan N. S., Arunraj S. P., Devanjan Sinha, Vinoth Babu Veedin Rajan, Vinoth Kumar Esthaki, Patrick D'Silva:
HSPIR: a manually annotated heat shock protein information resource. 2853-2855 - Ralf J. M. Weber, Eva Li, Jonathan Bruty, Shan He, Mark R. Viant:
MaConDa: a publicly accessible mass spectrometry contaminants database. 2856-2857 - William Speier, Michael F. Ochs:
Updating annotations with the distributed annotation system and the automated sequence annotation pipeline. 2858-2859
Volume 28, Number 22, November 2012
- Pan Tong, Kevin R. Coombes:
integIRTy: a method to identify genes altered in cancer by accounting for multiple mechanisms of regulation using item response theory. 2861-2869 - Binghang Liu, Jianying Yuan, Siu-Ming Yiu, Zhenyu Li, Yinlong Xie, Yanxiang Chen, Yujian Shi, Hao Zhang, Yingrui Li, Tak Wah Lam, Ruibang Luo:
COPE: an accurate k-mer-based pair-end reads connection tool to facilitate genome assembly. 2870-2874 - Tobias Marschall, Ivan G. Costa, Stefan Canzar, Markus Bauer, Gunnar W. Klau, Alexander Schliep, Alexander Schönhuth:
CLEVER: clique-enumerating variant finder. 2875-2882
- Peiyong Jiang, K. C. Allen Chan, Gary J. W. Liao, Yama W. L. Zheng, Tak Y. Leung, Rossa W. K. Chiu, Yuk Ming Dennis Lo, Hao Sun:
FetalQuant: deducing fractional fetal DNA concentration from massively parallel sequencing of DNA in maternal plasma. 2883-2890 - Marc J. Bonder, Sanne Abeln, Egija Zaura, Bernd W. Brandt:
Comparing clustering and pre-processing in taxonomy analysis. 2891-2897 - Xin Yang, John A. Todd, David Clayton, Chris Wallace:
Extra-binomial variation approach for analysis of pooled DNA sequencing data. 2898-2904
- Fuxiao Xin, Predrag Radivojac:
Post-translational modifications induce significant yet not extreme changes to protein structure. 2905-2913
- Wei Li, Tao Jiang:
Transcriptome assembly and isoform expression level estimation from biased RNA-Seq reads. 2914-2921 - Adam F. Allred, Hilary Renshaw, Scott Weaver, Robert B. Tesh, David Wang:
VIPR HMM: a hidden Markov model for detecting recombination with microbial detection microarrays. 2922-2929 - Michael Seifert, Sandra Cortijo, Maria Colomé-Tatché, Frank Johannes, François Roudier, Vincent Colot:
MeDIP-HMM: genome-wide identification of distinct DNA methylation states from high-density tiling arrays. 2930-2939 - Junfei Zhao, Shi-Hua Zhang, Ling-Yun Wu, Xiang-Sun Zhang:
Efficient methods for identifying mutated driver pathways in cancer. 2940-2947
- Hua Tan, Jiguang Bao, Xiaobo Zhou:
A novel missense-mutation-related feature extraction scheme for 'driver' mutation identification. 2948-2955
- Ting Huang, Zengyou He:
A linear programming model for protein inference problem in shotgun proteomics. 2956-2962 - Leon French, Suzanne Lane, Lydia Xu, Celia Siu, Cathy Kwok, Yiqi Chen, Claudia Krebs, Paul Pavlidis:
Application and evaluation of automated methods to extract neuroanatomical connectivity statements from free text. 2963-2970
- Tomasz Kalwarczyk, Marcin Tabaka, Robert Holyst:
Biologistics - Diffusion coefficients for complete proteome of Escherichia coli. 2971-2978
- Gary K. Chen, Kai Wang, Alex H. Stram, Eric M. Sobel, Kenneth Lange:
Mendel-GPU: haplotyping and genotype imputation on graphics processing units. 2979-2980 - Jean-Baptiste Cazier, Christopher C. Holmes, John Broxholme:
GREVE: Genomic Recurrent Event ViEwer to assist the identification of patterns across individual cancer samples. 2981-2982 - Mark D. Preston, Magnus Manske, Neil R. Horner, Samuel A. Assefa, Susana G. Campino, Sarah Auburn, Issaka Zongo, Jean-Bosco Ouedraogo, Francois Nosten, Timothy J. C. Anderson, Taane G. Clark:
VarB: a variation browsing and analysis tool for variants derived from next-generation sequencing data. 2983-2985
- Brent S. Pedersen, David A. Schwartz, Ivana V. Yang, Katerina J. Kechris:
Comb-p: software for combining, analyzing, grouping and correcting spatially correlated P-values. 2986-2988 - A. P. Jason de Koning, Wanjun Gu, Todd A. Castoe, David D. Pollock:
Phylogenetics, likelihood, evolution and complexity. 2989-2990 - Francesc Coll, Kim Mallard, Mark D. Preston, Stephen D. Bentley, Julian Parkhill, Ruth McNerney, Nigel J. Martin, Taane G. Clark:
SpolPred: rapid and accurate prediction of Mycobacterium tuberculosis spoligotypes from short genomic sequences. 2991-2993
- Joel Sjöstrand, Bengt Sennblad, Lars Arvestad, Jens Lagergren:
DLRS: gene tree evolution in light of a species tree. 2994-2995
- Ivan Kalev, Martin Mechelke, Klaus O. Kopec, Thomas Holder, Simeon Carstens, Michael Habeck:
CSB: a Python framework for structural bioinformatics. 2996-2997 - Jae-Seong Yang, Anne Campagna, Javier Delgado Blanco, Peter Vanhee, Luis Serrano, Christina Kiel:
SAPIN: A framework for the structural analysis of protein interaction networks. 2998-2999 - John Eargle, Zaida Luthey-Schulten:
NetworkView: 3D display and analysis of protein·RNA interaction networks. 3000-3001 - Emmanouil Athanasiadis, Zoe Cournia, George M. Spyrou:
ChemBioServer: a web-based pipeline for filtering, clustering and visualization of chemical compounds used in drug discovery. 3002-3003
- Jason Lloyd-Price, Abhishekh Gupta, Andre S. Ribeiro:
SGNS2: a compartmentalized stochastic chemical kinetics simulator for dynamic cell populations. 3004-3005
- Pablo Cordero, Julius B. Lucks, Rhiju Das:
An RNA Mapping DataBase for curating RNA structure mapping experiments. 3006-3008
- Tobias Pietzsch, Stephan Preibisch, Pavel Tomancak, Stephan Saalfeld:
ImgLib2 - generic image processing in Java. 3009-3011
Volume 28, Number 23, December 2012
- Philip J. Uren, Emad Bahrami Samani, Suzanne C. Burns, Mei Qiao, Fedor V. Karginov, Emily Hodges, Gregory J. Hannon, Jeremy R. Sanford, Luiz O. F. Penalva, Andrew D. Smith:
Site identification in high-throughput RNA-protein interaction data. 3013-3020 - Clemens Wrzodek, Johannes Eichner, Andreas Zell:
Pathway-based visualization of cross-platform microarray datasets. 3021-3026
- Heide Loehlein Fier, Sungho Won, Dmitry Prokopenko, Taofik AlChawa, Kerstin U. Ludwig, Rolf Fimmers, Edwin K. Silverman, Marcello Pagano, Elisabeth Mangold, Christoph Lange:
'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate. 3027-3033 - Nuno D. Mendes, Steffen Heyne, Ana T. Freitas, Marie-France Sagot, Rolf Backofen:
Navigating the unexplored seascape of pre-miRNA candidates in single-genome approaches. 3034-3041 - Dennis K. Gascoigne, Seth W. Cheetham, Pierre B. Cattenoz, Michael B. Clark, Paulo P. Amaral, Ryan J. Taft, Dagmar Wilhelm, Marcel E. Dinger, John S. Mattick:
Pinstripe: a suite of programs for integrating transcriptomic and proteomic datasets identifies novel proteins and improves differentiation of protein-coding and non-coding genes. 3042-3050 - Faraz Hach, Ibrahim Numanagic, Can Alkan, Süleyman Cenk Sahinalp:
SCALCE: boosting sequence compression algorithms using locally consistent encoding. 3051-3057
- Jana Sperschneider, Amitava Datta, Michael J. Wise:
Predicting pseudoknotted structures across two RNA sequences. 3058-3065 - Jesse Eickholt, Jianlin Cheng:
Predicting protein residue-residue contacts using deep networks and boosting. 3066-3072
- Yasir Rahmatallah, Frank Emmert-Streib, Galina V. Glazko:
Gene set analysis for self-contained tests: complex null and specific alternative hypotheses. 3073-3080
- Daniela Börnigen, Léon-Charles Tranchevent, Francisco Bonachela Capdevila, Koenraad Devriendt, Bart De Moor, Patrick De Causmaecker, Yves Moreau:
An unbiased evaluation of gene prioritization tools. 3081-3088 - Robert J. Flassig, Kai Sundmacher:
Optimal design of stimulus experiments for robust discrimination of biochemical reaction networks. 3089-3096 - Jole Costanza, Giovanni Carapezza, Claudio Angione, Pietro Liò, Giuseppe Nicosia:
Robust design of microbial strains. 3097-3104 - Rob Patro, Carl Kingsford:
Global network alignment using multiscale spectral signatures. 3105-3114 - David P. Nusinow, Adam Kiezun, Daniel J. O'Connell, Joel M. Chick, Yingzi Yue, Richard L. Maas, Steven Gygi, Shamil R. Sunyaev:
Network-based inference from complex proteomic mixtures using SNIPE. 3115-3122
- Kjell Johnson, Cen Guo, Mark Gosink, Vicky Wang, Manfred Hauben:
Multinomial modeling and an evaluation of common data-mining algorithms for identifying signals of disproportionate reporting in pharmacovigilance databases. 3123-3130
- Ming Hu, Ke Deng, Siddarth Selvaraj, Zhaohui S. Qin, Bing Ren, Jun S. Liu:
HiCNorm: removing biases in Hi-C data via Poisson regression. 3131-3133 - Alan Gray, I. Stewart, Albert Tenesa:
Advanced Complex Trait Analysis. 3134-3136 - Christian Frech, Caleb Choo, Nansheng Chen:
FeatureStack: Perl module for comparative visualization of gene features. 3137-3138 - Ross Lazarus, Antony Kaspi, Mark Ziemann, The Galaxy Team:
Creating reusable tools from scripts: the Galaxy Tool Factory. 3139-3140 - Chuang Ma, Hao Chen, Mingming Xin, Ruolin Yang, Xiangfeng Wang:
KGBassembler: a karyotype-based genome assembler for Brassicaceae species. 3141-3143
- Kazutaka Katoh, Martin C. Frith:
Adding unaligned sequences into an existing alignment using MAFFT and LAST. 3144-3146 - Chong-Jian Chen, Nicolas Servant, Joern Toedling, Alexis Sarazin, Antonin Marchais, Evelyne Duvernois-Berthet, Valérie Cognat, Vincent Colot, Olivier Voinnet, Edith Heard, Constance Ciaudo, Emmanuel Barillot:
ncPRO-seq: a tool for annotation and profiling of ncRNAs in sRNA-seq data. 3147-3149 - Limin Fu, Beifang Niu, Zhengwei Zhu, Sitao Wu, Weizhong Li:
CD-HIT: accelerated for clustering the next-generation sequencing data. 3150-3152
- Matthew N. McCall, Harris A. Jaffee, Rafael A. Irizarry:
fRMA ST: frozen robust multiarray analysis for Affymetrix Exon and Gene ST arrays. 3153-3154
- David Fange, Anel Mahmutovic, Johan Elf:
MesoRD 1.0: Stochastic reaction-diffusion simulations in the microscopic limit. 3155-3157
- Halil Kilicoglu, Dongwook Shin, Marcelo Fiszman, Graciela Rosemblat, Thomas C. Rindflesch:
SemMedDB: a PubMed-scale repository of biomedical semantic predications. 3158-3160 - Nicolas Parisot, Jérémie Denonfoux, Eric Dugat-Bony, Pierre Peyret, Eric Peyretaillade:
KASpOD - a web service for highly specific and explorative oligonucleotide design. 3161-3162
- Richard N. Smith, Jelena Aleksic, Daniela Butano, Adrian Carr, Sergio Contrino, Fengyuan Hu, Mike Lyne, Rachel Lyne, Alex Kalderimis, Kim Rutherford, Radek Stepan, Julie M. Sullivan, Matthew Wakeling, Xavier Watkins, Gos Micklem:
InterMine: a flexible data warehouse system for the integration and analysis of heterogeneous biological data. 3163-3165 - Alessandro Laganà, Alessio Paone, Dario Veneziano, Luciano Cascione, Pierluigi Gasparini, Stefania Carasi, Francesco Russo, Giovanni Nigita, Valentina Macca, Rosalba Giugno, Alfredo Pulvirenti, Dennis E. Shasha, Alfredo Ferro, Carlo Maria Croce:
miR-EdiTar: a database of predicted A-to-I edited miRNA target sites. 3166-3168
Volume 28, Number 24, December 2012
- Nuno A. Fonseca, Johan Rung, Alvis Brazma, John C. Marioni:
Tools for mapping high-throughput sequencing data. 3169-3177
- Cho-Yi Chen, Shui-Tein Chen, Hsueh-Fen Juan, Hsuan-Cheng Huang:
Lengthening of 3′UTR increases with morphological complexity in animal evolution. 3178-3181
- John Spencer Evans:
Aragonite-associated biomineralization proteins are disordered and contain interactive motifs. 3182-3185 - Darius Kazlauskas, Ceslovas Venclovas:
Two distinct SSB protein families in nucleo-cytoplasmic large DNA viruses. 3186-3190
- Jinyu Hu, David Zhiwei Gao:
Distinction immune genes of hepatitis-induced heptatocellular carcinoma. 3191-3194
- Jurgen F. Nijkamp, Marcel van den Broek, Jan-Maarten A. Geertman, Marcel J. T. Reinders, Jean-Marc Daran, Dick de Ridder:
De novo detection of copy number variation by co-assembly. 3195-3202
- Shaul Ashkenazi, Rotem Snir, Yanay Ofran:
Assessing the relationship between conservation of function and conservation of sequence using photosynthetic proteins. 3203-3210 - Evguenia Kopylova, Laurent Noé, Hélène Touzet:
SortMeRNA: fast and accurate filtering of ribosomal RNAs in metatranscriptomic data. 3211-3217 - Kengo Sato, Yuki Kato, Tatsuya Akutsu, Kiyoshi Asai, Yasubumi Sakakibara:
DAFS: simultaneous aligning and folding of RNA sequences via dual decomposition. 3218-3224 - Bas E. Dutilh, Robert Schmieder, James Nulton, Ben Felts, Peter Salamon, Robert A. Edwards, John Mokili:
Reference-independent comparative metagenomics using cross-assembly: crAss. 3225-3231 - Matteo Benelli, Chiara Pescucci, Giuseppina Marseglia, Marco Severgnini, Francesca Torricelli, Alberto Magi:
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript. 3232-3239 - Christof Angermüller, Andreas Biegert, Johannes Söding:
Discriminative modelling of context-specific amino acid substitution probabilities. 3240-3247
- Philippe Lemey, Vladimir N. Minin, Filip Bielejec, Sergei L. Kosakovsky Pond, Marc A. Suchard:
A counting renaissance: combining stochastic mapping and empirical Bayes to quickly detect amino acid sites under positive selection. 3248-3256
- Ian Walsh, Francesco Sirocco, Giovanni Minervini, Tomás Di Domenico, Carlo Ferrari, Silvio C. E. Tosatto:
RAPHAEL: recognition, periodicity and insertion assignment of solenoid protein structures. 3257-3264 - Mitul Saha, Marc C. Morais:
FOLD-EM: automated fold recognition in medium- and low-resolution (4-15 Å) electron density maps. 3265-3273 - David W. Ritchie, Anisah W. Ghoorah, Lazaros Mavridis, Vishwesh Venkatraman:
Fast protein structure alignment using Gaussian overlap scoring of backbone peptide fragment similarity. 3274-3281 - Dina Schneidman-Duhovny, Andrea Rossi, Agustin Avila-Sakar, Seung Joong Kim, Javier A. Velázquez-Muriel, Pavel Strop, Hong Liang, Kristin A. Krukenberg, Maofu Liao, Ho Min Kim, Solmaz Sobhanifar, Volker Dötsch, Arvind Rajpal, Jaume Pons, David A. Agard, Yifan Cheng, Andrej Sali:
A method for integrative structure determination of protein-protein complexes. 3282-3289
- Paul D. W. Kirk, Jim E. Griffin, Richard S. Savage, Zoubin Ghahramani, David L. Wild:
Bayesian correlated clustering to integrate multiple datasets. 3290-3297 - Thomas Thorne, Michael P. H. Stumpf:
Inference of temporally varying Bayesian Networks. 3298-3305
- Yongjun Piao, Minghao Piao, Kiejung Park, Keun Ho Ryu:
An ensemble correlation-based gene selection algorithm for cancer classification with gene expression data. 3306-3315
- Robert A. Edwards, Robert Olson, Terry Disz, Gordon D. Pusch, Veronika Vonstein, Rick Stevens, Ross A. Overbeek:
Real Time Metagenomics: Using k-mers to annotate metagenomes. 3316-3317 - András Aszódi:
MULTOVL: fast multiple overlaps of genomic regions. 3318-3319 - James A. Morris, Jeffrey C. Barrett:
Olorin: combining gene flow with exome sequencing in large family studies of complex disease. 3320-3321
- Phillipe Loher, Isidore Rigoutsos:
Interactive exploration of RNA22 microRNA target predictions. 3322-3323
- Yu Lin, Vaibhav Rajan, Bernard M. E. Moret:
TIBA: a tool for phylogeny inference from rearrangement data with bootstrap analysis. 3324-3325
- Xiuwen Zheng, David Levine, Jess Shen, Stephanie M. Gogarten, Cathy C. Laurie, Bruce S. Weir:
A high-performance computing toolset for relatedness and principal component analysis of SNP data. 3326-3328 - Stephanie M. Gogarten, Tushar Bhangale, Matthew P. Conomos, Cecelia A. Laurie, Caitlin P. McHugh, Ian S. Painter, Xiuwen Zheng, David R. Crosslin, David Levine, Thomas Lumley, Sarah C. Nelson, Ken Rice, Jess Shen, Rohit Swarnkar, Bruce S. Weir, Cathy C. Laurie:
GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies. 3329-3331 - Fabio Zanini, Richard A. Neher:
FFPopSim: an efficient forward simulation package for the evolution of large populations. 3332-3333
- Gong-Hua Li, Jing-Fei Huang:
CDRUG: a web server for predicting anticancer activity of chemical compounds. 3334-3335
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