Susan L. Slager

According to our database, Susan L. Slager authored at least 4 papers between 2014 and 2018.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of four.

2018

Comparative analysis of de novo assemblers for variation discovery in personal genomes.

Shulan Tian, Huihuang Yan, Eric W. Klee, Michael Kalmbach, Susan L. Slager

Briefings Bioinform., 2018

2016

Impact of post-alignment processing in variant discovery from whole exome data.

Shulan Tian, Huihuang Yan, Michael Kalmbach, Susan L. Slager

BMC Bioinform., 2016

2014

PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.

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

Bioinform., 2014

RVboost: RNA-seq variants prioritization using a boosting method.

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

Bioinform., 2014