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Journal Articles
- 2020
[j4]Zeynep Baskurt
, Scott Mastromatteo, Jiafen Gong, Richard F. Wintle, Stephen W. Scherer, Lisa J. Strug:
VikNGS: a C++ variant integration kit for next generation sequencing association analysis. Bioinform. 36(4): 1283-1285 (2020)- 2014
- [j3]Jeffrey R. MacDonald, Robert Ziman, Ryan K. C. Yuen, Lars Feuk, Stephen W. Scherer:
The Database of Genomic Variants: a curated collection of structural variation in the human genome. Nucleic Acids Res. 42(Database-Issue): 986-992 (2014) - 2011
- [j2]Takeshi Nishiyama, Kunihiko Takahashi, Toshiro Tango, Dalila Pinto, Stephen W. Scherer, Satoshi Takami, Hirohisa Kishino:
A Scan Statistic to Extract Causal Gene Clusters from Case-Control Genome-wide Rare CNV Data. BMC Bioinform. 12: 205 (2011) - 2003
- [j1]Alexander K. Hudek, Joseph Cheung, Andrew P. Boright, Stephen W. Scherer:
Genescript: DNA Sequence Annotation Pipeline. Bioinform. 19(9): 1177-1178 (2003)
Parts in Books or Collections
- 2002
- [p1]Lap Chee Tsui, Stephen W. Scherer:
Application Domains: The Human Genome Project. Essentials of Genomics and Bioinformatics 2002: 41-59
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