The browser you are using is not supported by this website. All versions of Internet Explorer are no longer supported, either by us or Microsoft (read more here: https://www.microsoft.com/en-us/microsoft-365/windows/end-of-ie-support).

Please use a modern browser to fully experience our website, such as the newest versions of Edge, Chrome, Firefox or Safari etc.

How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.

Author

  • Maija R J Kohonen-Corish
  • Jumana Y Al-Aama
  • Arleen D Auerbach
  • Myles Axton
  • Carol Isaacson Barash
  • Inge Bernstein
  • Christophe Béroud
  • John Burn
  • Fiona Cunningham
  • Garry R Cutting
  • Johan T den Dunnen
  • Marc S Greenblatt
  • Jim Kaput
  • Michael Katz
  • Annika Lindblom
  • Finlay Macrae
  • Donna Maglott
  • Gabriela Möslein
  • Sue Povey
  • Raj Ramesar
  • Sue Richards
  • Daniela Seminara
  • María-Jesús Sobrido
  • Sean Tavtigian
  • Graham Taylor
  • Mauno Vihinen
  • Ingrid Winship
  • Richard G H Cotton

Summary, in English

The third Human Variome Project (HVP) Meeting "Integration and Implementation" was held under UNESCO Patronage in Paris, France, at the UNESCO Headquarters May 10-14, 2010. The major aims of the HVP are the collection, curation, and distribution of all human genetic variation affecting health. The HVP has drawn together disparate groups, by country, gene of interest, and expertise, who are working for the common good with the shared goal of pushing the boundaries of the human variome and collaborating to avoid unnecessary duplication. The meeting addressed the 12 key areas that form the current framework of HVP activities: Ethics; Nomenclature and Standards; Publication, Credit and Incentives; Data Collection from Clinics; Overall Data Integration and Access-Peripheral Systems/Software; Data Collection from Laboratories; Assessment of Pathogenicity; Country Specific Collection; Translation to Healthcare and Personalized Medicine; Data Transfer, Databasing, and Curation; Overall Data Integration and Access-Central Systems; and Funding Mechanisms and Sustainability. In addition, three societies that support the goals and the mission of HVP also held their own Workshops with the view to advance disease-specific variation data collection and utilization: the International Society for Gastrointestinal Hereditary Tumours, the Micronutrient Genomics Project, and the Neurogenetics Consortium.

Publishing year

2010

Language

English

Pages

1374-1381

Publication/Series

Human Mutation

Volume

31

Issue

12

Document type

Journal article

Publisher

John Wiley & Sons Inc.

Topic

  • Medical Genetics

Keywords

  • Genome
  • Genetic: economics
  • Databases
  • Genetic Variation: genetics
  • Human: genetics
  • Mutation: ethics
  • Mutation: genetics

Status

Published

ISBN/ISSN/Other

  • ISSN: 1059-7794