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Journal Articles
- 2018
[j4]Shulan Tian, Huihuang Yan, Eric W. Klee, Michael Kalmbach, Susan L. Slager:
Comparative analysis of de novo assemblers for variation discovery in personal genomes. Briefings Bioinform. 19(5): 893-904 (2018)- 2016
- [j3]Shulan Tian, Huihuang Yan, Michael Kalmbach, Susan L. Slager:
Impact of post-alignment processing in variant discovery from whole exome data. BMC Bioinform. 17: 403 (2016) - 2014
- [j2]Chen Wang
, Jared Evans, Aditya Bhagwate, Naresh Prodduturi, Vivekananda Sarangi, Mridu Middha, Hugues Sicotte, Peter T. Vedell, Steven N. Hart, Gavin R. Oliver, Jean-Pierre A. Kocher, Matthew J. Maurer, Anne J. Novak, Susan L. Slager, James R. Cerhan, Yan W. Asmann:
PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data. Bioinform. 30(18): 2678-2680 (2014) - [j1]Chen Wang, Jaime I. Dávila, Saurabh Baheti, Aditya Bhagwate, Xue Wang, Jean-Pierre A. Kocher, Susan L. Slager, Andrew L. Feldman, Anne J. Novak, James R. Cerhan, E. Aubrey Thompson, Yan W. Asmann:
RVboost: RNA-seq variants prioritization using a boosting method. Bioinform. 30(23): 3414-3416 (2014)
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