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American Journal of Human Genetics
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February 14, 2017
Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy
Brent S Pedersen, Aaron R Quinlan
Methods in Molecular Biology (Clifton, N.J.)
|
January 10, 2012
Detection and interpretation of genomic structural variation in mammals
Ira M Hall, 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)
|
August 22, 2014
Poretools: a toolkit for analyzing nanopore sequence data
Nicholas J Loman, 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
|
February 20, 2015
Erratum: A reference bacterial genome dataset generated on the MinION(TM) portable single-molecule nanopore sequencer
Joshua Quick, Aaron R Quinlan, Nicholas J Loman
Biorxiv : the Preprint Server for Biology
|
February 9, 2026
The performance of genetic-constraint metrics varies significantly across the human noncoding genome
Peter McHale, Michael E Goldberg, Aaron R Quinlan
Gigascience
|
November 12, 2014
A reference bacterial genome dataset generated on the MinION™ portable single-molecule nanopore sequencer
Joshua Quick, Aaron R Quinlan, Nicholas J Loman
Biorxiv : the Preprint Server for Biology
|
May 10, 2023
Epistasis between mutator alleles contributes to germline mutation spectra variability in laboratory mice
Thomas A Sasani, Aaron R Quinlan, Kelley Harris
Elife
|
February 21, 2024
Epistasis between mutator alleles contributes to germline mutation spectrum variability in laboratory mice
Thomas A Sasani, Aaron R Quinlan, Kelley Harris
Page
of 11
Search research articles
Search
Showing results (11-20 of 104) with videos related to
Sort By:
Page
of 11
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
Methods in Molecular Biology (Clifton, N.J.)
|
January 10, 2012
Detection and interpretation of genomic structural variation in mammals
Ira M Hall, 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)
|
August 22, 2014
Poretools: a toolkit for analyzing nanopore sequence data
Nicholas J Loman, 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
|
February 20, 2015
Erratum: A reference bacterial genome dataset generated on the MinION(TM) portable single-molecule nanopore sequencer
Joshua Quick, Aaron R Quinlan, Nicholas J Loman
Biorxiv : the Preprint Server for Biology
|
February 9, 2026
The performance of genetic-constraint metrics varies significantly across the human noncoding genome
Peter McHale, Michael E Goldberg, Aaron R Quinlan
Gigascience
|
November 12, 2014
A reference bacterial genome dataset generated on the MinION™ portable single-molecule nanopore sequencer
Joshua Quick, Aaron R Quinlan, Nicholas J Loman
Biorxiv : the Preprint Server for Biology
|
May 10, 2023
Epistasis between mutator alleles contributes to germline mutation spectra variability in laboratory mice
Thomas A Sasani, Aaron R Quinlan, Kelley Harris
Elife
|
February 21, 2024
Epistasis between mutator alleles contributes to germline mutation spectrum variability in laboratory mice
Thomas A Sasani, Aaron R Quinlan, Kelley Harris
Page
of 11