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Bioinformatics (Oxford, England)|January 30, 2010
BEDTools: a flexible suite of utilities for comparing genomic featuresAaron R Quinlan, Ira M HallTrends in Genetics : TIG|November 19, 2011
Characterizing complex structural variation in germline and somatic genomesAaron R Quinlan, Ira M HallBioinformatics (Oxford, England)|November 3, 2017
Mosdepth: quick coverage calculation for genomes and exomesBrent S Pedersen, Aaron R QuinlanReproduction (Cambridge, England)|November 3, 2001
Nature of glycosylphosphatidylinositols produced by mouse embryonic stem cellsL R Quinlan, M T KaneProceedings of the IEEE. Institute of Electrical and Electronics Engineers|October 19, 2018
A parallel algorithm for N-way interval set intersectionRyan M Layer, Aaron R QuinlanGigascience|June 22, 2019
Duphold: scalable, depth-based annotation and curation of high-confidence structural variant callsBrent S Pedersen, Aaron R QuinlanOncogene|August 29, 2006
Cross-platform array comparative genomic hybridization meta-analysis separates hematopoietic and mesenchymal from epithelial tumorsK Jong, E Marchiori, A van der Vaart, et al.Biorxiv : the Preprint Server for Biology|November 22, 2024
Vcfexpress: flexible, rapid user-expressions to filter and format VCFsBrent S Pedersen, Aaron R QuinlanBioinformatics (Oxford, England)|February 7, 2017
cyvcf2: fast, flexible variant analysis with PythonBrent S Pedersen, Aaron R QuinlanAmerican 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 QuinlanPageof 33