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Jeffrey G Reid

Showing results (1-10 of 76) 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
Briefings in Bioinformatics|April 1, 2009
Expression profiling of microRNAs by deep sequencingChad J Creighton, Jeffrey G Reid, Preethi H Gunaratne
Bioinformatics (Oxford, England)|December 10, 2020
Sparse Project VCF: efficient encoding of population genotype matricesMichael F Lin, Xiaodong Bai, William J Salerno, et al.
Neurology. Genetics|October 5, 2019
Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainmentJoseph Park, Scott M Damrauer, Aris Baras, et al.
Nature Biotechnology|November 10, 2012
Genome interpretation and assembly-recent progress and next stepsShawn Baker, Anika Joecker, George Church, et al.
Bioinformatics (Oxford, England)|September 19, 2015
CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing dataJonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.
Genome Announcements|April 13, 2013
Complete Genome Sequence of Elephant Endotheliotropic Herpesvirus 1APaul D Ling, Jeffrey G Reid, Xiang Qin, et al.
Human Molecular Genetics|January 12, 2018
Large-scale exome datasets reveal a new class of adaptor-related protein complex 2 sigma subunit (AP2σ) mutations, located at the interface with the AP2 alpha subunit, that impair calcium-sensing receptor signallingCaroline M Gorvin, Raghu Metpally, Victoria J Stokes, et al.
Plos One|November 28, 2012
Mind the gap: upgrading genomes with Pacific Biosciences RS long-read sequencing technologyAdam C English, Stephen Richards, Yi Han, et al.
Genome Biology|June 5, 2007
Computational and transcriptional evidence for microRNAs in the honey bee genomeDaniel B Weaver, Juan M Anzola, Jay D Evans, et al.
Pageof 8

Showing results (1-10 of 76) with videos related to

Sort By:
Pageof 8
BMC Bioinformatics|June 12, 2014
PBHoney: identifying genomic variants via long-read discordance and interrupted mappingAdam C English, William J Salerno, Jeffrey G Reid
Briefings in Bioinformatics|April 1, 2009
Expression profiling of microRNAs by deep sequencingChad J Creighton, Jeffrey G Reid, Preethi H Gunaratne
Bioinformatics (Oxford, England)|December 10, 2020
Sparse Project VCF: efficient encoding of population genotype matricesMichael F Lin, Xiaodong Bai, William J Salerno, et al.
Neurology. Genetics|October 5, 2019
Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainmentJoseph Park, Scott M Damrauer, Aris Baras, et al.
Nature Biotechnology|November 10, 2012
Genome interpretation and assembly-recent progress and next stepsShawn Baker, Anika Joecker, George Church, et al.
Bioinformatics (Oxford, England)|September 19, 2015
CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing dataJonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.
Genome Announcements|April 13, 2013
Complete Genome Sequence of Elephant Endotheliotropic Herpesvirus 1APaul D Ling, Jeffrey G Reid, Xiang Qin, et al.
Human Molecular Genetics|January 12, 2018
Large-scale exome datasets reveal a new class of adaptor-related protein complex 2 sigma subunit (AP2σ) mutations, located at the interface with the AP2 alpha subunit, that impair calcium-sensing receptor signallingCaroline M Gorvin, Raghu Metpally, Victoria J Stokes, et al.
Plos One|November 28, 2012
Mind the gap: upgrading genomes with Pacific Biosciences RS long-read sequencing technologyAdam C English, Stephen Richards, Yi Han, et al.
Genome Biology|June 5, 2007
Computational and transcriptional evidence for microRNAs in the honey bee genomeDaniel B Weaver, Juan M Anzola, Jay D Evans, et al.
Pageof 8