Produção Nacional
Revisado por pares
Planning the Human Variome Project: The Spain report
2009; Wiley; Volume: 30; Issue: 4 Linguagem: Inglês
10.1002/humu.20972
ISSN1098-1004
AutoresJim Kaput, Richard G.H. Cotton, L Hardman, Michael S. Watson, Aida I. Al Aqeel, Jumana Y. Al‐Aama, Fahd Al‐Mulla, Santos Alonso, Stefan Aretz, Arleen D. Auerbach, Bharati Bapat, Inge Bernstein, Jong Bhak, Stacey Bléoo, Helmut Blöcker, Steven E. Brenner, John Burn, Mariona Bustamante, Rita Calzone, Anne Cambon‐Thomsen, Michele Cargill, Paola Carrera, Lawrence Cavedon, Yoon Shin Cho, Yeun‐Jun Chung, Mireille Claustres, Garry R. Cutting, Raymond Dalgleish, Johan T. den Dunnen, Carlos Bustamante, Steven F. Dobrowolski, Rosário Santos, Rosemary Ekong, Simon B. Flanagan, Paul Flicek, Yoichi Furukawa, Maurizio Genuardi, Ho Ghang, М. В. Голубенко, Marc S. Greenblatt, Ada Hamosh, John M. Hancock, Ross C. Hardison, Terence Harrison, Robert Hoffmann, Rania Horaitis, Heather J. Howard, Carol Isaacson Barash, Neskuts Izagirre, Jongsun Jung, Toshio Kojima, Sandrine Laradi, Yeon-Su Lee, Jong‐Young Lee, Vera Lúcia Gil‐da‐Silva‐Lopes, Finlay Macrae, Donna Maglott, Makia J. Marafie, Steven G. E. Marsh, Yoichi Matsubara, Ludwine M. Messiaen, Gabriela Möslein, Mihai G. Netea, Melissa Norton, Peter J. Oefner, William S. Oetting, James O’Leary, Ana María Oller Ramírez, Mark H. Paalman, Jillian S. Parboosingh, George P. Patrinos, Giuditta Perozzi, Ian Phillips, Sue Povey, S Prasad, Ming Qi, David J. Quin, Raj Ramesar, C. Sue Richards, Judy Savige, D. Scheible, Rodney J. Scott, Daniela Seminara, Elizabeth A. Shephard, Rolf H. Sijmons, Tim D. Smith, María-Jesús Sobrido, Toshihiro Tanaka, Sean V. Tavtigian, Graham R. Taylor, Jon W. Teague, Thoralf Töpel, Mollie Ullman-Culleré, Joji Utsunomiya, Henk J. van Kranen, Mauno Vihinen, Elizabeth Webb, Thomas K. Weber, Meredith Yeager, Young Il Yeom, Seon-Hee Yim, Hyang‐Sook Yoo,
Tópico(s)Genetics, Bioinformatics, and Biomedical Research
ResumoThe remarkable progress in characterizing the human genome sequence, exemplified by the Human Genome Project and the HapMap Consortium, has led to the perception that knowledge and the tools (e.g., microarrays) are sufficient for many if not most biomedical research efforts. A large amount of data from diverse studies proves this perception inaccurate at best, and at worst, an impediment for further efforts to characterize the variation in the human genome. Because variation in genotype and environment are the fundamental basis to understand phenotypic variability and heritability at the population level, identifying the range of human genetic variation is crucial to the development of personalized nutrition and medicine. The Human Variome Project (HVP; http://www.humanvariomeproject.org/) was proposed initially to systematically collect mutations that cause human disease and create a cyber infrastructure to link locus specific databases (LSDB). We report here the discussions and recommendations from the 2008 HVP planning meeting held in San Feliu de Guixols, Spain, in May 2008.
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