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Paper Details

Achieving high-sensitivity for clinical applications using augmented exome sequencing.
Genome Med
41
2015
ACE, ACE variant, ACMG secondary finding genes, InDels, NA12878, SNVs, augmented exome, disease-associated loci, exome, genes, genetic disease, genome, human, medically interpretable genes, protein-coding and noncoding sequences
Author NameAffiliation
Nan Leng
Deanna M Church
Deanna M Church
Shujun Luo
Shujun Luo
Christian D Haudenschild
Justin M ZookNational Institute of Standards and Technology
Marc SalitNational Institute of Standards and Technology
Stephen A Chervitz
Euan A AshleyCalifornia 94025 USA Center for Inherited Cardiovascular Disease, Stanford University School of Medicine
Michael SnyderStanford University School of Medicine
Michael SnyderStanford University School of Medicine
Russ B AltmanStanford University
Carlos D BustamanteStanford University School of Medicine
Carlos D BustamanteStanford University School of Medicine
Atul J ButteCalifornia 94025 USA Institute for Computational Health Sciences, University of California san francisco
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