Getting Ready for the Human Phenome Project: The 2012 Forum of the Human Variome Project
Identifieur interne : 000F03 ( Main/Merge ); précédent : 000F02; suivant : 000F04Getting Ready for the Human Phenome Project: The 2012 Forum of the Human Variome Project
Auteurs : William S. Oetting [États-Unis] ; Peter N. Robinson [Allemagne] ; Marc S. Greenblatt ; Richard G. Cotton [Australie] ; Tim Beck [Royaume-Uni] ; John C. Carey ; Sandra C. Doelken [Allemagne] ; Marta Girdea [Canada] ; Tudor Groza [Australie] ; Carol M. Hamilton ; Ada Hamosh [États-Unis] ; Berit Kerner [États-Unis] ; Jacqueline A. L. Macarthur [Royaume-Uni] ; Donna R. Maglott ; Barend Mons [Pays-Bas] ; Heidi L. Rehm [États-Unis] ; Paul N. Schofield [Royaume-Uni] ; Beverly A. Searle [Royaume-Uni] ; Damian Smedley [Royaume-Uni] ; Cynthia L. Smith ; Inge Thomsen Bernstein [Danemark] ; Andreas Zankl [Australie] ; Eric Y. Zhao [Canada]Source :
- [ 1059-7794 ]
Abstract
A forum of the Human Variome Project (HVP) was held as a satellite to the 2012 Annual Meeting of the American Society of Human Genetics in San Francisco, California. The theme of this meeting was “Getting Ready for the Human Phenome Project.” Understanding the genetic contribution to both rare single‐gene “Mendelian” disorders and more complex common diseases will require integration of research efforts among many fields and better defined phenotypes. The HVP is dedicated to bringing together researchers and research populations throughout the world to provide the resources to investigate the impact of genetic variation on disease. To this end, there needs to be a greater sharing of phenotype and genotype data. For this to occur, many databases that currently exist will need to become interoperable to allow for the combining of cohorts with similar phenotypes to increase statistical power for studies attempting to identify novel disease genes or causative genetic variants. Improved systems and tools that enhance the collection of phenotype data from clinicians are urgently needed. This meeting begins the HVP's effort toward this important goal.
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DOI: 10.1002/humu.22293
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Schofield</name><affiliation wicri:level="4"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge</wicri:regionArea><orgName type="university">Université de Cambridge</orgName><placeName><settlement type="city">Cambridge</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Angleterre de l'Est</region></placeName></affiliation></author><author><name sortKey="Searle, Beverly A" sort="Searle, Beverly A" uniqKey="Searle B" first="Beverly A." last="Searle">Beverly A. 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Smith</name><affiliation><wicri:noCountry code="subField">Harbor</wicri:noCountry></affiliation></author><author><name sortKey="Bernstein, Inge Thomsen" sort="Bernstein, Inge Thomsen" uniqKey="Bernstein I" first="Inge Thomsen" last="Bernstein">Inge Thomsen Bernstein</name><affiliation wicri:level="1"><country xml:lang="fr">Danemark</country><wicri:regionArea>The HNPCC‐register, Department of Gastroenterology and Clinical Research Center, Copenhagen University Hospital, Hvidovre</wicri:regionArea><wicri:noRegion>Hvidovre</wicri:noRegion></affiliation></author><author><name sortKey="Zankl, Andreas" sort="Zankl, Andreas" uniqKey="Zankl A" first="Andreas" last="Zankl">Andreas Zankl</name><affiliation wicri:level="1"><country xml:lang="fr">Australie</country><wicri:regionArea>University of Queensland's Centre for Clinical Research, The University of Queensland, Brisbane, Herston</wicri:regionArea><wicri:noRegion>Herston</wicri:noRegion></affiliation></author><author><name sortKey="Zhao, Eric Y" sort="Zhao, Eric Y" uniqKey="Zhao E" first="Eric Y." last="Zhao">Eric Y. Zhao</name><affiliation wicri:level="1"><country xml:lang="fr">Canada</country><wicri:regionArea>Department of Medical Genetics, The University of British Columbia, Vancouver</wicri:regionArea><wicri:noRegion>Vancouver</wicri:noRegion></affiliation></author></analytic><series><idno type="ISSN">1059-7794</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">1059-7794</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract">A forum of the Human Variome Project (HVP) was held as a satellite to the 2012 Annual Meeting of the American Society of Human Genetics in San Francisco, California. The theme of this meeting was “Getting Ready for the Human Phenome Project.” Understanding the genetic contribution to both rare single‐gene “Mendelian” disorders and more complex common diseases will require integration of research efforts among many fields and better defined phenotypes. The HVP is dedicated to bringing together researchers and research populations throughout the world to provide the resources to investigate the impact of genetic variation on disease. To this end, there needs to be a greater sharing of phenotype and genotype data. For this to occur, many databases that currently exist will need to become interoperable to allow for the combining of cohorts with similar phenotypes to increase statistical power for studies attempting to identify novel disease genes or causative genetic variants. Improved systems and tools that enhance the collection of phenotype data from clinicians are urgently needed. This meeting begins the HVP's effort toward this important goal.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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