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Marc Fiume

Showing results (1-10 of 19) with videos related to

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Bioinformatics (Oxford, England)|June 22, 2010
Savant: genome browser for high-throughput sequencing dataMarc Fiume, Vanessa Williams, Andrew Brook, et al.
Genome Research|September 1, 2010
Detecting copy number variation with mated short readsPaul Medvedev, Marc Fiume, Misko Dzamba, et al.
Plos Computational Biology|May 23, 2009
SHRiMP: accurate mapping of short color-space readsStephen M Rumble, Phil Lacroute, Adrian V Dalca, et al.
Nature Methods|January 28, 2014
Similarity network fusion for aggregating data types on a genomic scaleBo Wang, Aziz M Mezlini, Feyyaz Demir, et al.
Nucleic Acids Research|May 29, 2012
Savant Genome Browser 2: visualization and analysis for population-scale genomicsMarc Fiume, Eric J M Smith, Andrew Brook, et al.
Genome Research|December 4, 2012
iReckon: simultaneous isoform discovery and abundance estimation from RNA-seq dataAziz M Mezlini, Eric J M Smith, Marc Fiume, et al.
Human Mutation|May 3, 2013
PhenoTips: patient phenotyping software for clinical and research useMarta Girdea, Sergiu Dumitriu, Marc Fiume, et al.
Scientific Data|March 15, 2018
Simplifying research access to genomics and health data with Library CardsMoran 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 projectLena Dolman, Angela Page, Lawrence Babb, et al.
Cell Genomics|February 7, 2022
International federation of genomic medicine databases using GA4GH standardsAdrian Thorogood, Heidi L Rehm, Peter Goodhand, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|June 22, 2010
Savant: genome browser for high-throughput sequencing dataMarc Fiume, Vanessa Williams, Andrew Brook, et al.
Genome Research|September 1, 2010
Detecting copy number variation with mated short readsPaul Medvedev, Marc Fiume, Misko Dzamba, et al.
Plos Computational Biology|May 23, 2009
SHRiMP: accurate mapping of short color-space readsStephen M Rumble, Phil Lacroute, Adrian V Dalca, et al.
Nature Methods|January 28, 2014
Similarity network fusion for aggregating data types on a genomic scaleBo Wang, Aziz M Mezlini, Feyyaz Demir, et al.
Nucleic Acids Research|May 29, 2012
Savant Genome Browser 2: visualization and analysis for population-scale genomicsMarc Fiume, Eric J M Smith, Andrew Brook, et al.
Genome Research|December 4, 2012
iReckon: simultaneous isoform discovery and abundance estimation from RNA-seq dataAziz M Mezlini, Eric J M Smith, Marc Fiume, et al.
Human Mutation|May 3, 2013
PhenoTips: patient phenotyping software for clinical and research useMarta Girdea, Sergiu Dumitriu, Marc Fiume, et al.
Scientific Data|March 15, 2018
Simplifying research access to genomics and health data with Library CardsMoran 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 projectLena Dolman, Angela Page, Lawrence Babb, et al.
Cell Genomics|February 7, 2022
International federation of genomic medicine databases using GA4GH standardsAdrian Thorogood, Heidi L Rehm, Peter Goodhand, et al.
Pageof 2