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Andrew J Sharp

Showing results (11-20 of 85) with videos related to

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Bioinformatics (Oxford, England)|August 10, 2019
MsPAC: a tool for haplotype-phased structural variant detectionOscar L Rodriguez, Anna Ritz, Andrew J Sharp, et al.
Human Mutation|May 23, 2013
Rapid multiplexed genotyping of simple tandem repeats using capture and high-throughput sequencingAudrey Guilmatre, Gareth Highnam, Christelle Borel, et al.
JAMA Psychiatry|January 26, 2022
Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry BiobankRebecca Birnbaum, Behrang Mahjani, Ruth J F Loos, et al.
Genome Research|December 28, 2022
Genome-wide evaluation of the effect of short tandem repeat variation on local DNA methylationAlejandro Martin-Trujillo, Paras Garg, Nihir Patel, et al.
Annual Review of Genomics and Human Genetics|April 30, 2014
The genetics of microdeletion and microduplication syndromes: an updateCorey T Watson, Tomas Marques-Bonet, Andrew J Sharp, et al.
BMC Genomics|May 1, 2023
Small open reading frames: a comparative genetics approach to validationNiyati Jain, Felix Richter, Ivan Adzhubei, et al.
Plos Genetics|December 15, 2015
DNA Methylation: Insights into Human EvolutionIrene Hernando-Herraez, Raquel Garcia-Perez, Andrew J Sharp, et al.
European Journal of Human Genetics : EJHG|August 4, 2016
Copy number variation of the REXO1L1 gene cluster; euchromatic deletion variant or susceptibility factor?John C K Barber, Andrew J Sharp, Edward J Hollox, et al.
American Journal of Human Genetics|May 21, 2026
A phenome-wide association study of CNVs genotyped from genome sequencing read depth in the UK BiobankParas Garg, Bharati Jadhav, Mariya Shadrina, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndromeArnaud Duchon, Matthieu Raveau, Claire Chevalier, et al.
Pageof 9

Showing results (11-20 of 85) with videos related to

Sort By:
Pageof 9
Bioinformatics (Oxford, England)|August 10, 2019
MsPAC: a tool for haplotype-phased structural variant detectionOscar L Rodriguez, Anna Ritz, Andrew J Sharp, et al.
Human Mutation|May 23, 2013
Rapid multiplexed genotyping of simple tandem repeats using capture and high-throughput sequencingAudrey Guilmatre, Gareth Highnam, Christelle Borel, et al.
JAMA Psychiatry|January 26, 2022
Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry BiobankRebecca Birnbaum, Behrang Mahjani, Ruth J F Loos, et al.
Genome Research|December 28, 2022
Genome-wide evaluation of the effect of short tandem repeat variation on local DNA methylationAlejandro Martin-Trujillo, Paras Garg, Nihir Patel, et al.
Annual Review of Genomics and Human Genetics|April 30, 2014
The genetics of microdeletion and microduplication syndromes: an updateCorey T Watson, Tomas Marques-Bonet, Andrew J Sharp, et al.
BMC Genomics|May 1, 2023
Small open reading frames: a comparative genetics approach to validationNiyati Jain, Felix Richter, Ivan Adzhubei, et al.
Plos Genetics|December 15, 2015
DNA Methylation: Insights into Human EvolutionIrene Hernando-Herraez, Raquel Garcia-Perez, Andrew J Sharp, et al.
European Journal of Human Genetics : EJHG|August 4, 2016
Copy number variation of the REXO1L1 gene cluster; euchromatic deletion variant or susceptibility factor?John C K Barber, Andrew J Sharp, Edward J Hollox, et al.
American Journal of Human Genetics|May 21, 2026
A phenome-wide association study of CNVs genotyped from genome sequencing read depth in the UK BiobankParas Garg, Bharati Jadhav, Mariya Shadrina, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndromeArnaud Duchon, Matthieu Raveau, Claire Chevalier, et al.
Pageof 9