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Human genomics

Showing results (311-320 of 1,251) with videos related to

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Human Genomics|January 4, 2026
The global burden of ischemic heart disease attributable to trans fatty acid in 204 countries and territories, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023XueNa Wang, Gang Liang
Human Genomics|May 14, 2020
An investigation of genetic polymorphisms in heparan sulfate proteoglycan core proteins and key modification enzymes in an Australian Caucasian multiple sclerosis populationRachel K Okolicsanyi, Julia Bluhm, Cassandra Miller, et al.
Human Genomics|February 8, 2011
RGD: a comparative genomics platformMary Shimoyama, Jennifer R Smith, Tom Hayman, et al.
Human Genomics|April 7, 2010
An introduction to effective use of enrichment analysis softwareHannah Tipney, Lawrence Hunter
Human Genomics|July 24, 2010
The other lives of ribosomal proteinsRital B Bhavsar, Leah N Makley, Panagiotis A Tsonis
Human Genomics|November 26, 2010
Prospects for the automated extraction of mutation data from the scientific literaturePeter D Stenson, David N Cooper
Human Genomics|November 26, 2010
A survey of statistical software for analysing RNA-seq dataDexiang Gao, Jihye Kim, Hyunmin Kim, et al.
Human Genomics|September 18, 2010
General considerations for integrating pharmacogenomics into mainstream medical practiceGeorge P Patrinos
Human Genomics|September 18, 2010
Endothelial nitric oxide synthase gene polymorphisms -786T > C and 894G > T in coronary artery bypass graft surgery patientsGeorgia Ragia, Eleftherios Nikolaidis, Anna Tavridou, et al.
Human Genomics|September 18, 2010
A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variationAnis Karimpour-Fard, Laura Dumas, Tzulip Phang, et al.
Pageof 126

Showing results (311-320 of 1,251) with videos related to

Sort By:
Pageof 126
Human Genomics|January 4, 2026
The global burden of ischemic heart disease attributable to trans fatty acid in 204 countries and territories, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023XueNa Wang, Gang Liang
Human Genomics|May 14, 2020
An investigation of genetic polymorphisms in heparan sulfate proteoglycan core proteins and key modification enzymes in an Australian Caucasian multiple sclerosis populationRachel K Okolicsanyi, Julia Bluhm, Cassandra Miller, et al.
Human Genomics|February 8, 2011
RGD: a comparative genomics platformMary Shimoyama, Jennifer R Smith, Tom Hayman, et al.
Human Genomics|April 7, 2010
An introduction to effective use of enrichment analysis softwareHannah Tipney, Lawrence Hunter
Human Genomics|July 24, 2010
The other lives of ribosomal proteinsRital B Bhavsar, Leah N Makley, Panagiotis A Tsonis
Human Genomics|November 26, 2010
Prospects for the automated extraction of mutation data from the scientific literaturePeter D Stenson, David N Cooper
Human Genomics|November 26, 2010
A survey of statistical software for analysing RNA-seq dataDexiang Gao, Jihye Kim, Hyunmin Kim, et al.
Human Genomics|September 18, 2010
General considerations for integrating pharmacogenomics into mainstream medical practiceGeorge P Patrinos
Human Genomics|September 18, 2010
Endothelial nitric oxide synthase gene polymorphisms -786T > C and 894G > T in coronary artery bypass graft surgery patientsGeorgia Ragia, Eleftherios Nikolaidis, Anna Tavridou, et al.
Human Genomics|September 18, 2010
A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variationAnis Karimpour-Fard, Laura Dumas, Tzulip Phang, et al.
Pageof 126