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David N Cooper

Showing results (161-170 of 398) with videos related to

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Human Genetics|January 28, 2022
Trypsinogen (PRSS1 and PRSS2) gene dosage correlates with pancreatitis risk across genetic and transgenic studies: a systematic review and re-analysisWen-Bin Zou, David N Cooper, Emmanuelle Masson, et al.
Genome Biology|March 19, 2013
DDIG-in: discriminating between disease-associated and neutral non-frameshifting micro-indelsHuiying Zhao, Yuedong Yang, Hai Lin, et al.
Genome Biology|January 20, 2017
iRegNet3D: three-dimensional integrated regulatory network for the genomic analysis of coding and non-coding disease mutationsSiqi Liang, Nathaniel D Tippens, Yaoda Zhou, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 24, 2012
Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type XChee-Seng Ku, David N Cooper, Mengchu Wu, et al.
Nucleic Acids Research|May 3, 2019
SeqTailor: a user-friendly webserver for the extraction of DNA or protein sequences from next-generation sequencing dataPeng Zhang, Bertrand Boisson, Peter D Stenson, et al.
Human Genomics|July 2, 2014
Ranking non-synonymous single nucleotide polymorphisms based on disease conceptsHashem A Shihab, Julian Gough, Matthew Mort, et al.
Human Molecular Genetics|January 18, 2014
Impact of human pathogenic micro-insertions and micro-deletions on post-transcriptional regulationXinjun Zhang, Hai Lin, Huiying Zhao, et al.
Genome Medicine|May 14, 2024
The landscape of rare genetic variation associated with inflammatory bowel disease and Parkinson's disease comorbidityMeltem Ece Kars, Yiming Wu, Peter D Stenson, et al.
Human Mutation|July 19, 2002
Assessing the relative importance of the biophysical properties of amino acid substitutions associated with human genetic diseaseBent N Terp, David N Cooper, Inge T Christensen, et al.
Human Mutation|May 21, 2015
Disclosing the Hidden Structure and Underlying Mutational Mechanism of a Novel Type of Duplication CNV Responsible for Hereditary Multiple OsteochondromasPeiqiang Su, Ye Wang, David N Cooper, et al.
Pageof 40

Showing results (161-170 of 398) with videos related to

Sort By:
Pageof 40
Human Genetics|January 28, 2022
Trypsinogen (PRSS1 and PRSS2) gene dosage correlates with pancreatitis risk across genetic and transgenic studies: a systematic review and re-analysisWen-Bin Zou, David N Cooper, Emmanuelle Masson, et al.
Genome Biology|March 19, 2013
DDIG-in: discriminating between disease-associated and neutral non-frameshifting micro-indelsHuiying Zhao, Yuedong Yang, Hai Lin, et al.
Genome Biology|January 20, 2017
iRegNet3D: three-dimensional integrated regulatory network for the genomic analysis of coding and non-coding disease mutationsSiqi Liang, Nathaniel D Tippens, Yaoda Zhou, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 24, 2012
Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type XChee-Seng Ku, David N Cooper, Mengchu Wu, et al.
Nucleic Acids Research|May 3, 2019
SeqTailor: a user-friendly webserver for the extraction of DNA or protein sequences from next-generation sequencing dataPeng Zhang, Bertrand Boisson, Peter D Stenson, et al.
Human Genomics|July 2, 2014
Ranking non-synonymous single nucleotide polymorphisms based on disease conceptsHashem A Shihab, Julian Gough, Matthew Mort, et al.
Human Molecular Genetics|January 18, 2014
Impact of human pathogenic micro-insertions and micro-deletions on post-transcriptional regulationXinjun Zhang, Hai Lin, Huiying Zhao, et al.
Genome Medicine|May 14, 2024
The landscape of rare genetic variation associated with inflammatory bowel disease and Parkinson's disease comorbidityMeltem Ece Kars, Yiming Wu, Peter D Stenson, et al.
Human Mutation|July 19, 2002
Assessing the relative importance of the biophysical properties of amino acid substitutions associated with human genetic diseaseBent N Terp, David N Cooper, Inge T Christensen, et al.
Human Mutation|May 21, 2015
Disclosing the Hidden Structure and Underlying Mutational Mechanism of a Novel Type of Duplication CNV Responsible for Hereditary Multiple OsteochondromasPeiqiang Su, Ye Wang, David N Cooper, et al.
Pageof 40