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William J Salerno

Showing results (1-10 of 22) with videos related to

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BMC Bioinformatics|June 12, 2014
PBHoney: identifying genomic variants via long-read discordance and interrupted mappingAdam C English, William J Salerno, Jeffrey G Reid
Nucleic Acids Research|June 25, 2004
MONSTER: inferring non-covalent interactions in macromolecular structures from atomic coordinate dataWilliam J Salerno, Samuel M Seaver, Brian R Armstrong, et al.
Bioinformatics (Oxford, England)|December 10, 2020
Sparse Project VCF: efficient encoding of population genotype matricesMichael F Lin, Xiaodong Bai, William J Salerno, et al.
Cell|June 6, 2003
Solution structure of a CUE-ubiquitin complex reveals a conserved mode of ubiquitin bindingRichard S Kang, Cynthia M Daniels, Smitha A Francis, et al.
Gigascience|December 21, 2020
Parliament2: Accurate structural variant calling at scaleSamantha Zarate, Andrew Carroll, Medhat Mahmoud, et al.
Genome Research|April 3, 2021
Optimized sample selection for cost-efficient long-read population sequencingT Rhyker Ranallo-Benavidez, Zachary Lemmon, Sebastian Soyk, et al.
Bioinformatics (Oxford, England)|April 21, 2019
VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing ProjectYuk Yee Leung, Otto Valladares, Yi-Fan Chou, et al.
Bioinformatics (Oxford, England)|October 24, 2018
VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing ProjectYuk Yee Leung, Otto Valladares, Yi-Fan Chou, et al.
BMC Genomics|October 7, 2017
SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing readsOliver A Hampton, Adam C English, Mark Wang, et al.
Nature Genetics|September 25, 2024
Yield of genetic association signals from genomes, exomes and imputation in the UK BiobankSheila M Gaynor, Tyler Joseph, Xiaodong Bai, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
BMC Bioinformatics|June 12, 2014
PBHoney: identifying genomic variants via long-read discordance and interrupted mappingAdam C English, William J Salerno, Jeffrey G Reid
Nucleic Acids Research|June 25, 2004
MONSTER: inferring non-covalent interactions in macromolecular structures from atomic coordinate dataWilliam J Salerno, Samuel M Seaver, Brian R Armstrong, et al.
Bioinformatics (Oxford, England)|December 10, 2020
Sparse Project VCF: efficient encoding of population genotype matricesMichael F Lin, Xiaodong Bai, William J Salerno, et al.
Cell|June 6, 2003
Solution structure of a CUE-ubiquitin complex reveals a conserved mode of ubiquitin bindingRichard S Kang, Cynthia M Daniels, Smitha A Francis, et al.
Gigascience|December 21, 2020
Parliament2: Accurate structural variant calling at scaleSamantha Zarate, Andrew Carroll, Medhat Mahmoud, et al.
Genome Research|April 3, 2021
Optimized sample selection for cost-efficient long-read population sequencingT Rhyker Ranallo-Benavidez, Zachary Lemmon, Sebastian Soyk, et al.
Bioinformatics (Oxford, England)|April 21, 2019
VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing ProjectYuk Yee Leung, Otto Valladares, Yi-Fan Chou, et al.
Bioinformatics (Oxford, England)|October 24, 2018
VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing ProjectYuk Yee Leung, Otto Valladares, Yi-Fan Chou, et al.
BMC Genomics|October 7, 2017
SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing readsOliver A Hampton, Adam C English, Mark Wang, et al.
Nature Genetics|September 25, 2024
Yield of genetic association signals from genomes, exomes and imputation in the UK BiobankSheila M Gaynor, Tyler Joseph, Xiaodong Bai, et al.
Pageof 3