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Aaron R Quinlan

Showing results (21-30 of 104) with videos related to

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Bioinformatics (Oxford, England)|December 21, 2014
Population-based structural variation discovery with Hydra-MultiMichael R Lindberg, Ira M Hall, Aaron R Quinlan
NAR Genomics and Bioinformatics|December 20, 2024
Improved characterization of 3' single-cell RNA-seq libraries with paired-end avidity sequencingJohn T Chamberlin, Austin E Gillen, Aaron R Quinlan
Bioinformatics (Oxford, England)|September 28, 2011
Pybedtools: a flexible Python library for manipulating genomic datasets and annotationsRyan K Dale, Brent S Pedersen, Aaron R Quinlan
Genome Biology|June 3, 2016
Vcfanno: fast, flexible annotation of genetic variantsBrent S Pedersen, Ryan M Layer, Aaron R Quinlan
BMC Bioinformatics|November 17, 2022
Annotation of structural variants with reported allele frequencies and related metrics from multiple datasets using SVAFotateThomas J Nicholas, Michael J Cormier, Aaron R Quinlan
Biorxiv : the Preprint Server for Biology|July 19, 2024
Improved characterization of single-cell RNA-seq libraries with paired-end avidity sequencingJohn T Chamberlin, Austin E Gillen, Aaron R Quinlan
Plos Computational Biology|July 23, 2013
GEMINI: integrative exploration of genetic variation and genome annotationsUmadevi Paila, Brad A Chapman, Rory Kirchner, et al.
Genetics|March 25, 2026
The selective dynamics of interruptions at short tandem repeatsMichael E Goldberg, Harriet Dashnow, Kelley Harris, et al.
Genome Biology|June 28, 2014
LUMPY: a probabilistic framework for structural variant discoveryRyan M Layer, Colby Chiang, Aaron R Quinlan, et al.
Genome Research|February 14, 2024
Differences in molecular sampling and data processing explain variation among single-cell and single-nucleus RNA-seq experimentsJohn T Chamberlin, Younghee Lee, Gabor T Marth, et al.
Pageof 11

Showing results (21-30 of 104) with videos related to

Sort By:
Pageof 11
Bioinformatics (Oxford, England)|December 21, 2014
Population-based structural variation discovery with Hydra-MultiMichael R Lindberg, Ira M Hall, Aaron R Quinlan
NAR Genomics and Bioinformatics|December 20, 2024
Improved characterization of 3' single-cell RNA-seq libraries with paired-end avidity sequencingJohn T Chamberlin, Austin E Gillen, Aaron R Quinlan
Bioinformatics (Oxford, England)|September 28, 2011
Pybedtools: a flexible Python library for manipulating genomic datasets and annotationsRyan K Dale, Brent S Pedersen, Aaron R Quinlan
Genome Biology|June 3, 2016
Vcfanno: fast, flexible annotation of genetic variantsBrent S Pedersen, Ryan M Layer, Aaron R Quinlan
BMC Bioinformatics|November 17, 2022
Annotation of structural variants with reported allele frequencies and related metrics from multiple datasets using SVAFotateThomas J Nicholas, Michael J Cormier, Aaron R Quinlan
Biorxiv : the Preprint Server for Biology|July 19, 2024
Improved characterization of single-cell RNA-seq libraries with paired-end avidity sequencingJohn T Chamberlin, Austin E Gillen, Aaron R Quinlan
Plos Computational Biology|July 23, 2013
GEMINI: integrative exploration of genetic variation and genome annotationsUmadevi Paila, Brad A Chapman, Rory Kirchner, et al.
Genetics|March 25, 2026
The selective dynamics of interruptions at short tandem repeatsMichael E Goldberg, Harriet Dashnow, Kelley Harris, et al.
Genome Biology|June 28, 2014
LUMPY: a probabilistic framework for structural variant discoveryRyan M Layer, Colby Chiang, Aaron R Quinlan, et al.
Genome Research|February 14, 2024
Differences in molecular sampling and data processing explain variation among single-cell and single-nucleus RNA-seq experimentsJohn T Chamberlin, Younghee Lee, Gabor T Marth, et al.
Pageof 11