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DePristo

Showing results (31-40 of 59) with videos related to

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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.
Human Molecular Genetics|January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Nature Genetics|July 22, 2011
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarctionJessica Shea, Vineeta Agarwala, Anthony A Philippakis, et al.
Current Protocols in Bioinformatics|November 29, 2014
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipelineGeraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, et al.
Genome Biology|July 2, 2014
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequencesVincenza Colonna, Qasim Ayub, Yuan Chen, et al.
Nature Genetics|June 14, 2011
Variation in genome-wide mutation rates within and between human familiesDonald F Conrad, Jonathan E M Keebler, Mark A DePristo, et al.
Nature Genetics|April 12, 2011
A framework for variation discovery and genotyping using next-generation DNA sequencing dataMark A DePristo, Eric Banks, Ryan Poplin, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
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.
Human Molecular Genetics|January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Nature Genetics|July 22, 2011
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarctionJessica Shea, Vineeta Agarwala, Anthony A Philippakis, et al.
Current Protocols in Bioinformatics|November 29, 2014
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipelineGeraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, et al.
Genome Biology|July 2, 2014
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequencesVincenza Colonna, Qasim Ayub, Yuan Chen, et al.
Nature Genetics|June 14, 2011
Variation in genome-wide mutation rates within and between human familiesDonald F Conrad, Jonathan E M Keebler, Mark A DePristo, et al.
Nature Genetics|April 12, 2011
A framework for variation discovery and genotyping using next-generation DNA sequencing dataMark A DePristo, Eric Banks, Ryan Poplin, et al.
Pageof 6