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BMC Bioinformatics
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June 12, 2014
PBHoney: identifying genomic variants via long-read discordance and interrupted mapping
Adam C English, William J Salerno, Jeffrey G Reid
Briefings in Bioinformatics
|
April 1, 2009
Expression profiling of microRNAs by deep sequencing
Chad J Creighton, Jeffrey G Reid, Preethi H Gunaratne
Bioinformatics (Oxford, England)
|
December 10, 2020
Sparse Project VCF: efficient encoding of population genotype matrices
Michael F Lin, Xiaodong Bai, William J Salerno, et al.
Neurology. Genetics
|
October 5, 2019
Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainment
Joseph Park, Scott M Damrauer, Aris Baras, et al.
Nature Biotechnology
|
November 10, 2012
Genome interpretation and assembly-recent progress and next steps
Shawn 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 data
Jonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.
Genome Announcements
|
April 13, 2013
Complete Genome Sequence of Elephant Endotheliotropic Herpesvirus 1A
Paul 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 signalling
Caroline 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 technology
Adam C English, Stephen Richards, Yi Han, et al.
Genome Biology
|
June 5, 2007
Computational and transcriptional evidence for microRNAs in the honey bee genome
Daniel B Weaver, Juan M Anzola, Jay D Evans, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 76) with videos related to
Sort By:
Page
of 8
BMC Bioinformatics
|
June 12, 2014
PBHoney: identifying genomic variants via long-read discordance and interrupted mapping
Adam C English, William J Salerno, Jeffrey G Reid
Briefings in Bioinformatics
|
April 1, 2009
Expression profiling of microRNAs by deep sequencing
Chad J Creighton, Jeffrey G Reid, Preethi H Gunaratne
Bioinformatics (Oxford, England)
|
December 10, 2020
Sparse Project VCF: efficient encoding of population genotype matrices
Michael F Lin, Xiaodong Bai, William J Salerno, et al.
Neurology. Genetics
|
October 5, 2019
Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainment
Joseph Park, Scott M Damrauer, Aris Baras, et al.
Nature Biotechnology
|
November 10, 2012
Genome interpretation and assembly-recent progress and next steps
Shawn 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 data
Jonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.
Genome Announcements
|
April 13, 2013
Complete Genome Sequence of Elephant Endotheliotropic Herpesvirus 1A
Paul 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 signalling
Caroline 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 technology
Adam C English, Stephen Richards, Yi Han, et al.
Genome Biology
|
June 5, 2007
Computational and transcriptional evidence for microRNAs in the honey bee genome
Daniel B Weaver, Juan M Anzola, Jay D Evans, et al.
Page
of 8