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Bioinformatics (Oxford, England)
|
June 22, 2010
Savant: genome browser for high-throughput sequencing data
Marc Fiume, Vanessa Williams, Andrew Brook, et al.
Genome Research
|
September 1, 2010
Detecting copy number variation with mated short reads
Paul Medvedev, Marc Fiume, Misko Dzamba, et al.
Plos Computational Biology
|
May 23, 2009
SHRiMP: accurate mapping of short color-space reads
Stephen M Rumble, Phil Lacroute, Adrian V Dalca, et al.
Nature Methods
|
January 28, 2014
Similarity network fusion for aggregating data types on a genomic scale
Bo Wang, Aziz M Mezlini, Feyyaz Demir, et al.
Nucleic Acids Research
|
May 29, 2012
Savant Genome Browser 2: visualization and analysis for population-scale genomics
Marc Fiume, Eric J M Smith, Andrew Brook, et al.
Genome Research
|
December 4, 2012
iReckon: simultaneous isoform discovery and abundance estimation from RNA-seq data
Aziz M Mezlini, Eric J M Smith, Marc Fiume, et al.
Human Mutation
|
May 3, 2013
PhenoTips: patient phenotyping software for clinical and research use
Marta Girdea, Sergiu Dumitriu, Marc Fiume, et al.
Scientific Data
|
March 15, 2018
Simplifying research access to genomics and health data with Library Cards
Moran N Cabili, Knox Carey, Stephanie O M Dyke, et al.
Human Mutation
|
October 13, 2018
ClinGen advancing genomic data-sharing standards as a GA4GH driver project
Lena Dolman, Angela Page, Lawrence Babb, et al.
Cell Genomics
|
February 7, 2022
International federation of genomic medicine databases using GA4GH standards
Adrian Thorogood, Heidi L Rehm, Peter Goodhand, et al.
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Search research articles
Search
Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Bioinformatics (Oxford, England)
|
June 22, 2010
Savant: genome browser for high-throughput sequencing data
Marc Fiume, Vanessa Williams, Andrew Brook, et al.
Genome Research
|
September 1, 2010
Detecting copy number variation with mated short reads
Paul Medvedev, Marc Fiume, Misko Dzamba, et al.
Plos Computational Biology
|
May 23, 2009
SHRiMP: accurate mapping of short color-space reads
Stephen M Rumble, Phil Lacroute, Adrian V Dalca, et al.
Nature Methods
|
January 28, 2014
Similarity network fusion for aggregating data types on a genomic scale
Bo Wang, Aziz M Mezlini, Feyyaz Demir, et al.
Nucleic Acids Research
|
May 29, 2012
Savant Genome Browser 2: visualization and analysis for population-scale genomics
Marc Fiume, Eric J M Smith, Andrew Brook, et al.
Genome Research
|
December 4, 2012
iReckon: simultaneous isoform discovery and abundance estimation from RNA-seq data
Aziz M Mezlini, Eric J M Smith, Marc Fiume, et al.
Human Mutation
|
May 3, 2013
PhenoTips: patient phenotyping software for clinical and research use
Marta Girdea, Sergiu Dumitriu, Marc Fiume, et al.
Scientific Data
|
March 15, 2018
Simplifying research access to genomics and health data with Library Cards
Moran N Cabili, Knox Carey, Stephanie O M Dyke, et al.
Human Mutation
|
October 13, 2018
ClinGen advancing genomic data-sharing standards as a GA4GH driver project
Lena Dolman, Angela Page, Lawrence Babb, et al.
Cell Genomics
|
February 7, 2022
International federation of genomic medicine databases using GA4GH standards
Adrian Thorogood, Heidi L Rehm, Peter Goodhand, et al.
Page
of 2