Human Variome Project country nodes: documenting genetic information within a country. Academic Article uri icon

Overview

abstract

  • The Human Variome Project (http://www.humanvariomeproject.org) is an international effort aiming to systematically collect and share information on all human genetic variation. The two main pillars of this effort are gene/disease-specific databases and a network of Human Variome Project Country Nodes. The latter are nationwide efforts to document the genomic variation reported within a specific population. The development and successful operation of the Human Variome Project Country Nodes are of utmost importance to the success of Human Variome Project's aims and goals because they not only allow the genetic burden of disease to be quantified in different countries, but also provide diagnosticians and researchers access to an up-to-date resource that will assist them in their daily clinical practice and biomedical research, respectively. Here, we report the discussions and recommendations that resulted from the inaugural meeting of the International Confederation of Countries Advisory Council, held on 12th December 2011, during the 2011 Human Variome Project Beijing Meeting. We discuss the steps necessary to maximize the impact of the Country Node effort for developing regional and country-specific clinical genetics resources and summarize a few well-coordinated genetic data collection initiatives that would serve as paradigms for similar projects.

authors

  • Patrinos, George P
  • Smith, Timothy D
  • Howard, Heather
  • Al-Mulla, Fahd
  • Chouchane, Lotfi
  • Hadjisavvas, Andreas
  • Hamed, Sherifa A
  • Li, Xi-Tao
  • Marafie, Makia
  • Ramesar, Rajkumar S
  • Ramos, Feliciano J
  • de Ravel, Thomy
  • El-Ruby, Mona O
  • Shrestha, Tilak Ram
  • Sobrido, María-Jesús
  • Tadmouri, Ghazi
  • Witsch-Baumgartner, Martina
  • Zilfalil, Bin Alwi
  • Auerbach, Arleen
  • Carpenter, Kevin
  • Cutting, Garry R
  • Dung, Vu Chi
  • Grody, Wayne
  • Hasler, Julia
  • Jorde, Lynn
  • Kaput, Jim
  • Macek, Milan
  • Matsubara, Yoichi
  • Padilla, Carmancita
  • Robinson, Helen
  • Rojas-Martinez, Augusto
  • Taylor, Graham R
  • Vihinen, Mauno
  • Weber, Tom
  • Burn, John
  • Qi, Ming
  • Cotton, Richard G H
  • Rimoin, David

publication date

  • July 18, 2012

Research

keywords

  • Genetic Variation
  • Genome, Human
  • Human Genome Project

Identity

Scopus Document Identifier

  • 84867475839

Digital Object Identifier (DOI)

  • 10.1002/humu.22147

PubMed ID

  • 22753370

Additional Document Info

volume

  • 33

issue

  • 11