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Kiran V Garimella

Showing results (1-10 of 16) with videos related to

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Bioinformatics (Oxford, England)|March 20, 2018
Integrating long-range connectivity information into de Bruijn graphsIsaac Turner, Kiran V Garimella, Zamin Iqbal, et al.
Bioinformatics (Oxford, England)|January 3, 2025
Fast and exact gap-affine partial order alignment with POASTALucas R van Dijk, Abigail L Manson, Ashlee M Earl, et al.
Genome Biology and Evolution|August 5, 2022
A Beary Good Genome: Haplotype-Resolved, Chromosome-Level Assembly of the Brown Bear (Ursus arctos)Ellie E Armstrong, Blair W Perry, Yongqing Huang, et al.
Genome Research|August 21, 2020
Detection of simple and complex de novo mutations with multiple reference sequencesKiran V Garimella, Zamin Iqbal, Michael A Krause, 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.
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.
Nature Communications|January 3, 2024
Integrative genotyping of cancer and immune phenotypes by long-read sequencingLivius Penter, Mehdi Borji, Adi Nagler, 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 Biotechnology|June 8, 2023
High-throughput RNA isoform sequencing using programmed cDNA concatenationAziz M Al'Khafaji, Jonathan T Smith, Kiran V Garimella, 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 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|March 20, 2018
Integrating long-range connectivity information into de Bruijn graphsIsaac Turner, Kiran V Garimella, Zamin Iqbal, et al.
Bioinformatics (Oxford, England)|January 3, 2025
Fast and exact gap-affine partial order alignment with POASTALucas R van Dijk, Abigail L Manson, Ashlee M Earl, et al.
Genome Biology and Evolution|August 5, 2022
A Beary Good Genome: Haplotype-Resolved, Chromosome-Level Assembly of the Brown Bear (Ursus arctos)Ellie E Armstrong, Blair W Perry, Yongqing Huang, et al.
Genome Research|August 21, 2020
Detection of simple and complex de novo mutations with multiple reference sequencesKiran V Garimella, Zamin Iqbal, Michael A Krause, 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.
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.
Nature Communications|January 3, 2024
Integrative genotyping of cancer and immune phenotypes by long-read sequencingLivius Penter, Mehdi Borji, Adi Nagler, 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 Biotechnology|June 8, 2023
High-throughput RNA isoform sequencing using programmed cDNA concatenationAziz M Al'Khafaji, Jonathan T Smith, Kiran V Garimella, 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 2