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Nucleic Acids Research
|
June 25, 2013
Loss of heterozygosity preferentially occurs in early replicating regions in cancer genomes
Brent S Pedersen, Subhajyoti De
Nucleic Acids Research
|
October 27, 2022
Echtvar: compressed variant representation for rapid annotation and filtering of SNPs and indels
Brent S Pedersen, Jeroen de Ridder
Bioinformatics (Oxford, England)
|
November 3, 2017
Mosdepth: quick coverage calculation for genomes and exomes
Brent S Pedersen, Aaron R Quinlan
Biorxiv : the Preprint Server for Biology
|
November 22, 2024
Vcfexpress: flexible, rapid user-expressions to filter and format VCFs
Brent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)
|
February 7, 2017
cyvcf2: fast, flexible variant analysis with Python
Brent 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 Peddy
Brent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)
|
May 3, 2018
hts-nim: scripting high-performance genomic analyses
Brent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)
|
March 4, 2025
Vcfexpress: flexible, rapid user-expressions to filter and format VCFs
Brent S Pedersen, Aaron R Quinlan
Gigascience
|
June 22, 2019
Duphold: scalable, depth-based annotation and curation of high-confidence structural variant calls
Brent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)
|
February 8, 2011
Gobe: an interactive, web-based tool for comparative genomic visualization
Brent S Pedersen, Haibao Tang, Michael Freeling
Page
of 7
Search research articles
Search
Showing results (1-10 of 65) with videos related to
Sort By:
Page
of 7
Nucleic Acids Research
|
June 25, 2013
Loss of heterozygosity preferentially occurs in early replicating regions in cancer genomes
Brent S Pedersen, Subhajyoti De
Nucleic Acids Research
|
October 27, 2022
Echtvar: compressed variant representation for rapid annotation and filtering of SNPs and indels
Brent S Pedersen, Jeroen de Ridder
Bioinformatics (Oxford, England)
|
November 3, 2017
Mosdepth: quick coverage calculation for genomes and exomes
Brent S Pedersen, Aaron R Quinlan
Biorxiv : the Preprint Server for Biology
|
November 22, 2024
Vcfexpress: flexible, rapid user-expressions to filter and format VCFs
Brent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)
|
February 7, 2017
cyvcf2: fast, flexible variant analysis with Python
Brent 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 Peddy
Brent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)
|
May 3, 2018
hts-nim: scripting high-performance genomic analyses
Brent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)
|
March 4, 2025
Vcfexpress: flexible, rapid user-expressions to filter and format VCFs
Brent S Pedersen, Aaron R Quinlan
Gigascience
|
June 22, 2019
Duphold: scalable, depth-based annotation and curation of high-confidence structural variant calls
Brent S Pedersen, Aaron R Quinlan
Bioinformatics (Oxford, England)
|
February 8, 2011
Gobe: an interactive, web-based tool for comparative genomic visualization
Brent S Pedersen, Haibao Tang, Michael Freeling
Page
of 7