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Molecular Biology and Evolution|April 30, 2010
Low-complexity regions in Plasmodium falciparum: missing links in the evolution of an extreme genomeMartine M Zilversmit, Sarah K Volkman, Mark A DePristo, et al.Plos Computational Biology|July 19, 2012
Efficiency and power as a function of sequence coverage, SNP array density, and imputationJason Flannick, Joshua M Korn, Pierre Fontanillas, et al.Structure (London, England : 1993)|August 15, 2006
Knowledge-based real-space explorations for low-resolution structure determinationNicholas Furnham, Andrew S Doré, Dimitri Y Chirgadze, et al.Nature Biotechnology|February 22, 2022
Using deep learning to annotate the protein universeMaxwell L Bileschi, David Belanger, Drew H Bryant, et al.Genome Research|July 21, 2010
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing dataAaron McKenna, Matthew Hanna, Eric Banks, et al.Nature|November 7, 2012
An integrated map of genetic variation from 1,092 human genomes, Goncalo R Abecasis, Adam Auton, et al.BMC Genomics|January 20, 2011
Next-generation sequencing for HLA typing of class I lociRachel L Erlich, Xiaoming Jia, Scott Anderson, et al.Bioinformatics (Oxford, England)|June 10, 2011
The variant call format and VCFtoolsPetr Danecek, Adam Auton, Goncalo Abecasis, et al.European Journal of Human Genetics : EJHG|November 24, 2016
A framework for the detection of de novo mutations in family-based sequencing dataLaurent C Francioli, Mircea Cretu-Stancu, Kiran V Garimella, et al.Nature Biotechnology|September 25, 2018
A universal SNP and small-indel variant caller using deep neural networksRyan Poplin, Pi-Chuan Chang, David Alexander, et al.Pageof 5