Comprehensive variation discovery in single human genomes
Neil Weisenfeld(Broad Institute), David B. Jaffe(GlobeImmune (United States)), Eric S. Lander(Broad Institute), Brian Sogoloff(Broad Institute), Chad Nusbaum(Broad Institute), Diana Tabbaa(Broad Institute), Ryan Hegarty(Broad Institute), Shuangye Yin(Broad Institute), Iain MacCallum(Broad Institute), Louise Williams(Broad Institute), Ted Sharpe(Broad Institute), Laurie Holmes(Broad Institute), Carsten Russ(Broad Institute), Bayo Lau(Broad Institute)
Cited by 247
Related Papers
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
|Proceedings of the National Academy of Sciences|2005|56.5k
Initial sequencing and analysis of the human genome
|Nature|2001|24.6k
Full-length transcriptome assembly from RNA-Seq data without a reference genome
|Nature Biotechnology|2011|22.7k
Model-based Analysis of ChIP-Seq (MACS)
|Genome biology|2008|20k
A global reference for human genetic variation
|Nature|2015|19.9k