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David N Cooper

Showing results (211-220 of 398) with videos related to

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Briefings in Bioinformatics|May 13, 2017
Mutational signatures and mutable motifs in cancer genomesIgor B Rogozin, Youri I Pavlov, Alexander Goncearenco, et al.
Genome Biology|January 24, 2014
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicingMatthew Mort, Timothy Sterne-Weiler, Biao Li, et al.
Human Mutation|June 18, 2011
Single base-pair substitutions at the translation initiation sites of human genes as a cause of inherited diseaseAndreas Wolf, Amke Caliebe, Nick S T Thomas, et al.
Bioinformatics (Oxford, England)|September 8, 2009
Automated inference of molecular mechanisms of disease from amino acid substitutionsBiao Li, Vidhya G Krishnan, Matthew E Mort, et al.
Genome Research|August 9, 2008
Abundance and length of simple repeats in vertebrate genomes are determined by their structural propertiesAlbino Bacolla, Jacquelynn E Larson, Jack R Collins, et al.
Human Genetics|December 20, 2005
Polymorphic micro-inversions contribute to the genomic variability of humans and chimpanzeesJustyna M Szamalek, David N Cooper, Werner Schempp, et al.
Human Genetics|July 12, 2018
Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequencesAnna Summerer, Victor-Felix Mautner, Meena Upadhyaya, et al.
Human Mutation|June 28, 2012
Microattribution and nanopublication as means to incentivize the placement of human genome variation data into the public domainGeorge P Patrinos, David N Cooper, Erik van Mulligen, et al.
Genomic Medicine|September 24, 2008
Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 geneLyndon G Rosser, Shane McKee, David S Millar, et al.
Lipids in Health and Disease|August 7, 2023
The East Asian-specific LPL p.Ala288Thr (c.862G > A) missense variant exerts a mild effect on protein functionYuepeng Hu, Guofu Zhang, Qi Yang, et al.
Pageof 40

Showing results (211-220 of 398) with videos related to

Sort By:
Pageof 40
Briefings in Bioinformatics|May 13, 2017
Mutational signatures and mutable motifs in cancer genomesIgor B Rogozin, Youri I Pavlov, Alexander Goncearenco, et al.
Genome Biology|January 24, 2014
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicingMatthew Mort, Timothy Sterne-Weiler, Biao Li, et al.
Human Mutation|June 18, 2011
Single base-pair substitutions at the translation initiation sites of human genes as a cause of inherited diseaseAndreas Wolf, Amke Caliebe, Nick S T Thomas, et al.
Bioinformatics (Oxford, England)|September 8, 2009
Automated inference of molecular mechanisms of disease from amino acid substitutionsBiao Li, Vidhya G Krishnan, Matthew E Mort, et al.
Genome Research|August 9, 2008
Abundance and length of simple repeats in vertebrate genomes are determined by their structural propertiesAlbino Bacolla, Jacquelynn E Larson, Jack R Collins, et al.
Human Genetics|December 20, 2005
Polymorphic micro-inversions contribute to the genomic variability of humans and chimpanzeesJustyna M Szamalek, David N Cooper, Werner Schempp, et al.
Human Genetics|July 12, 2018
Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequencesAnna Summerer, Victor-Felix Mautner, Meena Upadhyaya, et al.
Human Mutation|June 28, 2012
Microattribution and nanopublication as means to incentivize the placement of human genome variation data into the public domainGeorge P Patrinos, David N Cooper, Erik van Mulligen, et al.
Genomic Medicine|September 24, 2008
Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 geneLyndon G Rosser, Shane McKee, David S Millar, et al.
Lipids in Health and Disease|August 7, 2023
The East Asian-specific LPL p.Ala288Thr (c.862G > A) missense variant exerts a mild effect on protein functionYuepeng Hu, Guofu Zhang, Qi Yang, et al.
Pageof 40