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Brent S Pedersen

Showing results (1-10 of 65) with videos related to

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Nucleic Acids Research|June 25, 2013
Loss of heterozygosity preferentially occurs in early replicating regions in cancer genomesBrent S Pedersen, Subhajyoti De
Nucleic Acids Research|October 27, 2022
Echtvar: compressed variant representation for rapid annotation and filtering of SNPs and indelsBrent S Pedersen, Jeroen de Ridder
Bioinformatics (Oxford, England)|November 3, 2017
Mosdepth: quick coverage calculation for genomes and exomesBrent S Pedersen, Aaron R Quinlan
Biorxiv : the Preprint Server for Biology|November 22, 2024
Vcfexpress: flexible, rapid user-expressions to filter and format VCFsBrent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)|February 7, 2017
cyvcf2: fast, flexible variant analysis with PythonBrent S Pedersen, Aaron R Quinlan
American Journal of Human Genetics|February 14, 2017
Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with PeddyBrent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)|May 3, 2018
hts-nim: scripting high-performance genomic analysesBrent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)|March 4, 2025
Vcfexpress: flexible, rapid user-expressions to filter and format VCFsBrent S Pedersen, Aaron R Quinlan
Gigascience|June 22, 2019
Duphold: scalable, depth-based annotation and curation of high-confidence structural variant callsBrent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)|February 8, 2011
Gobe: an interactive, web-based tool for comparative genomic visualizationBrent S Pedersen, Haibao Tang, Michael Freeling
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
Nucleic Acids Research|June 25, 2013
Loss of heterozygosity preferentially occurs in early replicating regions in cancer genomesBrent S Pedersen, Subhajyoti De
Nucleic Acids Research|October 27, 2022
Echtvar: compressed variant representation for rapid annotation and filtering of SNPs and indelsBrent S Pedersen, Jeroen de Ridder
Bioinformatics (Oxford, England)|November 3, 2017
Mosdepth: quick coverage calculation for genomes and exomesBrent S Pedersen, Aaron R Quinlan
Biorxiv : the Preprint Server for Biology|November 22, 2024
Vcfexpress: flexible, rapid user-expressions to filter and format VCFsBrent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)|February 7, 2017
cyvcf2: fast, flexible variant analysis with PythonBrent S Pedersen, Aaron R Quinlan
American Journal of Human Genetics|February 14, 2017
Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with PeddyBrent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)|May 3, 2018
hts-nim: scripting high-performance genomic analysesBrent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)|March 4, 2025
Vcfexpress: flexible, rapid user-expressions to filter and format VCFsBrent S Pedersen, Aaron R Quinlan
Gigascience|June 22, 2019
Duphold: scalable, depth-based annotation and curation of high-confidence structural variant callsBrent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)|February 8, 2011
Gobe: an interactive, web-based tool for comparative genomic visualizationBrent S Pedersen, Haibao Tang, Michael Freeling
Pageof 7