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BMC Genomics
|
July 11, 2013
Variant discovery in targeted resequencing using whole genome amplified DNA
Amit R Indap, Regina Cole, Christina L Runge, et al.
BMC Bioinformatics
|
December 17, 2005
Analysis of concordance of different haplotype block partitioning algorithms
Amit R Indap, Gabor T Marth, Craig A Struble, et al.
Bioinformatics (Oxford, England)
|
January 15, 2013
Scotty: a web tool for designing RNA-Seq experiments to measure differential gene expression
Michele A Busby, Chip Stewart, Chase A Miller, et al.
Bioinformatics (Oxford, England)
|
April 16, 2011
BamTools: a C++ API and toolkit for analyzing and managing BAM files
Derek W Barnett, Erik K Garrison, Aaron R Quinlan, et al.
Plos One
|
March 7, 2014
MOSAIK: a hash-based algorithm for accurate next-generation sequencing short-read mapping
Wan-Ping Lee, Michael P Stromberg, Alistair Ward, et al.
Genome Medicine
|
March 27, 2021
OncoGEMINI: software for investigating tumor variants from multiple biopsies with integrated cancer annotations
Thomas J Nicholas, Michael J Cormier, Xiaomeng Huang, et al.
Nature Methods
|
January 9, 2018
GIGGLE: a search engine for large-scale integrated genome analysis
Ryan M Layer, Brent S Pedersen, Tonya DiSera, et al.
Genome Biology
|
August 28, 2014
SubcloneSeeker: a computational framework for reconstructing tumor clone structure for cancer variant interpretation and prioritization
Yi Qiao, Aaron R Quinlan, Amir A Jazaeri, et al.
BMC Bioinformatics
|
November 20, 2012
Copy Number Variation detection from 1000 Genomes Project exon capture sequencing data
Jiantao Wu, Krzysztof R Grzeda, Chip Stewart, et al.
BMC Genomics
|
September 18, 2014
Tangram: a comprehensive toolbox for mobile element insertion detection
Jiantao Wu, Wan-Ping Lee, Alistair Ward, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 61) with videos related to
Sort By:
Page
of 7
BMC Genomics
|
July 11, 2013
Variant discovery in targeted resequencing using whole genome amplified DNA
Amit R Indap, Regina Cole, Christina L Runge, et al.
BMC Bioinformatics
|
December 17, 2005
Analysis of concordance of different haplotype block partitioning algorithms
Amit R Indap, Gabor T Marth, Craig A Struble, et al.
Bioinformatics (Oxford, England)
|
January 15, 2013
Scotty: a web tool for designing RNA-Seq experiments to measure differential gene expression
Michele A Busby, Chip Stewart, Chase A Miller, et al.
Bioinformatics (Oxford, England)
|
April 16, 2011
BamTools: a C++ API and toolkit for analyzing and managing BAM files
Derek W Barnett, Erik K Garrison, Aaron R Quinlan, et al.
Plos One
|
March 7, 2014
MOSAIK: a hash-based algorithm for accurate next-generation sequencing short-read mapping
Wan-Ping Lee, Michael P Stromberg, Alistair Ward, et al.
Genome Medicine
|
March 27, 2021
OncoGEMINI: software for investigating tumor variants from multiple biopsies with integrated cancer annotations
Thomas J Nicholas, Michael J Cormier, Xiaomeng Huang, et al.
Nature Methods
|
January 9, 2018
GIGGLE: a search engine for large-scale integrated genome analysis
Ryan M Layer, Brent S Pedersen, Tonya DiSera, et al.
Genome Biology
|
August 28, 2014
SubcloneSeeker: a computational framework for reconstructing tumor clone structure for cancer variant interpretation and prioritization
Yi Qiao, Aaron R Quinlan, Amir A Jazaeri, et al.
BMC Bioinformatics
|
November 20, 2012
Copy Number Variation detection from 1000 Genomes Project exon capture sequencing data
Jiantao Wu, Krzysztof R Grzeda, Chip Stewart, et al.
BMC Genomics
|
September 18, 2014
Tangram: a comprehensive toolbox for mobile element insertion detection
Jiantao Wu, Wan-Ping Lee, Alistair Ward, et al.
Page
of 7