Stephen W. Scherer

According to our database, Stephen W. Scherer authored at least 6 papers between 2002 and 2025.

Collaborative distances:

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

2025

Near-Lossless Model Compression Enables Longer Context Inference in DNA Large Language Models.

Rui Zhu, Xiaopu Zhou, Haixu Tang, Stephen W. Scherer, Lucila Ohno-Machado

CoRR, November, 2025

2020

VikNGS: a C++ variant integration kit for next generation sequencing association analysis.

Zeynep Baskurt, Scott Mastromatteo, Jiafen Gong, Richard F. Wintle, Stephen W. Scherer, Lisa J. Strug

Bioinform., 2020

2014

The Database of Genomic Variants: a curated collection of structural variation in the human genome.

Jeffrey R. MacDonald, Robert Ziman, Ryan K. C. Yuen, Lars Feuk, Stephen W. Scherer

Nucleic Acids Res., 2014

2011

A Scan Statistic to Extract Causal Gene Clusters from Case-Control Genome-wide Rare CNV Data.

Takeshi Nishiyama, Kunihiko Takahashi, Toshiro Tango, Dalila Pinto, Stephen W. Scherer, Satoshi Takami, Hirohisa Kishino

BMC Bioinform., 2011

2003

Genescript: DNA Sequence Annotation Pipeline.

Alexander K. Hudek, Joseph Cheung, Andrew P. Boright, Stephen W. Scherer

Bioinform., 2003

2002

Application Domains: The Human Genome Project.

Lap Chee Tsui, Stephen W. Scherer

Proceedings of the Essentials of Genomics and Bioinformatics, 2002