967 citations · 1.4k across the 2 of their papers we have counts for
2 papers
q-bio.GN2013★ 967 cited
Integrating sequencing datasets to form highly confident SNP and indel genotype calls for a whole human genome
Justin M. Zook, Brad Chapman, Jason Wang +4
Clinical adoption of human genome sequencing requires methods with known accuracy of genotype calls at millions or billions of positions across a genome. Previous work showing disc…
q-bio.GN2013★ 481 cited
GEMINI: integrative exploration of genetic variation and genome annotations
Uma Paila, Brad Chapman, Rory Kirchner +1
Modern DNA sequencing technologies enable geneticists to rapidly identify genetic variation among many human genomes. However, isolating the minority of variants underlying disease…