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Nature Reviews. Genetics|August 19, 2011
Needles in stacks of needles: finding disease-causal variants in a wealth of genomic dataGregory M Cooper, Jay ShendureHuman Molecular Genetics|August 2, 2021
Linking genome variants to disease: scalable approaches to test the functional impact of human mutationsGregory M FindlayNature Biotechnology|November 10, 2012
The expanding scope of DNA sequencingJay Shendure, Erez Lieberman AidenScience (New York, N.Y.)|September 26, 2015
The origins, determinants, and consequences of human mutationsJay Shendure, Joshua M AkeyGenome Biology|September 13, 2002
Computational discovery of sense-antisense transcription in the human and mouse genomesJay Shendure, George M ChurchNature|September 14, 2018
Accurate classification of BRCA1 variants with saturation genome editingGregory M Findlay, Riza M Daza, Beth Martin, et al.Genome Research|November 6, 2014
Large-scale genomic sequencing of extraintestinal pathogenic Escherichia coli strainsStephen J Salipante, David J Roach, Jacob O Kitzman, et al.Nature Protocols|September 2, 2016
The power of multiplexed functional analysis of genetic variantsMolly Gasperini, Lea Starita, Jay ShendurePageof 43