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Reece K Hart

Showing results (1-10 of 13) with videos related to

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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|February 13, 2009
Unison: an integrated platform for computational biology discoveryReece K Hart, Kiran Mukhyala
Plos One|December 3, 2020
SeqRepo: A system for managing local collections of biological sequencesReece K Hart, Andreas Prlić
Human Mutation|October 3, 2017
VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptionsPeter J Freeman, Reece K Hart, Liam J Gretton, et al.
Bioinformatics (Oxford, England)|October 3, 2014
A Python package for parsing, validating, mapping and formatting sequence variants using HGVS nomenclatureReece K Hart, Rudolph Rico, Emily Hare, et al.
Human Mutation|January 22, 2016
Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation SocietyWilliam S Oetting, Steven E Brenner, Anthony J Brookes, et al.
Genome Medicine|December 20, 2024
HGVS Nomenclature 2024: improvements to community engagement, usability, and computabilityReece K Hart, Ivo F A C Fokkema, Marina DiStefano, et al.
Human Mutation|March 3, 2016
HGVS Recommendations for the Description of Sequence Variants: 2016 UpdateJohan T den Dunnen, Raymond Dalgleish, Donna R Maglott, et al.
Human Mutation|August 22, 2018
hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 UpdateMeng Wang, Keith M Callenberg, Raymond Dalgleish, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 21, 2022
Development and application of a computable genotype model in the GA4GH Variation Representation SpecificationWesley Goar, Lawrence Babb, Srikar Chamala, et al.
Genome Medicine|November 6, 2016
Somatic cancer variant curation and harmonization through consensus minimum variant level dataDeborah I Ritter, Sameek Roychowdhury, Angshumoy Roy, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|February 13, 2009
Unison: an integrated platform for computational biology discoveryReece K Hart, Kiran Mukhyala
Plos One|December 3, 2020
SeqRepo: A system for managing local collections of biological sequencesReece K Hart, Andreas Prlić
Human Mutation|October 3, 2017
VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptionsPeter J Freeman, Reece K Hart, Liam J Gretton, et al.
Bioinformatics (Oxford, England)|October 3, 2014
A Python package for parsing, validating, mapping and formatting sequence variants using HGVS nomenclatureReece K Hart, Rudolph Rico, Emily Hare, et al.
Human Mutation|January 22, 2016
Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation SocietyWilliam S Oetting, Steven E Brenner, Anthony J Brookes, et al.
Genome Medicine|December 20, 2024
HGVS Nomenclature 2024: improvements to community engagement, usability, and computabilityReece K Hart, Ivo F A C Fokkema, Marina DiStefano, et al.
Human Mutation|March 3, 2016
HGVS Recommendations for the Description of Sequence Variants: 2016 UpdateJohan T den Dunnen, Raymond Dalgleish, Donna R Maglott, et al.
Human Mutation|August 22, 2018
hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 UpdateMeng Wang, Keith M Callenberg, Raymond Dalgleish, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 21, 2022
Development and application of a computable genotype model in the GA4GH Variation Representation SpecificationWesley Goar, Lawrence Babb, Srikar Chamala, et al.
Genome Medicine|November 6, 2016
Somatic cancer variant curation and harmonization through consensus minimum variant level dataDeborah I Ritter, Sameek Roychowdhury, Angshumoy Roy, et al.
Pageof 2