Some features of the site may not work correctly.The HapMap Web site at http://www.hapmap.org is the primary portal to genotype data produced as part of the International Haplotype Map Project. As the goal of the project is solely to identify patterns of genetic variation, no medical or other phenotypic information will be included. It will be an ongoing challenge to avoid misinterpretations or misuses of results from studies that use the HapMap. 2019 Winter;12(6):80-94.Wu FL, Strand AI, Cox LA, Ober C, Wall JD, Moorjani P, Przeworski M.PLoS Biol.
The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. The International HapMap Project Web site. The HapMap Web site provides researchers with a number of tools that allow them to analyze the data as well as download data for local analyses. Box 6128, Downtown Station, Montréal, Québec, H3C 3J7, Canada,Department of Anthropology, University of Oklahoma, 455 West Lindsey Street, Norman, Oklahoma, 73019, USA,Vanderbilt University, Center for Genetics and Health Policy, 507 Light Hall, Nashville, Tennessee, 37232, USA,Ellen Wright Clayton, Vivian Ota Wang, Ellen Wright Clayton (co-chair) & Vivian Ota Wang,Wellcome Trust, 183 Euston Road, London, NW1 2BE, UK,Jessica Watkin, Karen Kennedy, Michael G. Dunn, Richard Seabrook, Barbara Skene, John G. Stewart & Patricia Spallone,Washington University School of Medicine, Genome Sequencing Center, Box 8501, 4444 Forest Park Avenue, St Louis, Missouri, 63108, USA,Whitehead Institute/MIT Center for Genome Research, 9 Cambridge Center, Massachusetts, 02142, Cambridge, USA,Chinese Academy of Sciences, 52 Sanlihe Road, Beijing, 100864, China,Chinese Ministry of Science and Technology, 15B Fuxing Road, Beijing, 100862, China,Genome Canada, 150 Metcalfe Street, Suite 2100, Ottawa, Ontario, K2P 1P1, Canada,McGill University, Office of Technology Transfer, 3550 University Street, Montréal, Québec, H3A 2A7, Canada,Génome Québec, 630 Boulevard René-Lévesque Ouest, Montréal, Québec, H3B 1S6, Canada,Ministry of Education, Culture, Sports, Science and Technology, 3-2-2 Kasumigaseki, Chiyodaku, Tokyo, Japan,Hiraki and Associates, Toranomon No. Please enable it to take advantage of the complete set of features!Clipboard, Search History, and several other advanced features are temporarily unavailable.National Center for Biotechnology Information,Unable to load your collection due to an error,Unable to load your delegates due to an error.Nature. The HapMap Web site provides researchers with a number of tools that allow them to analyze the data as well as & Altshuler, D. Quality and completeness of SNP databases.Jeffreys, A. J., Kauppi, L. & Neumann, R. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex.Gabriel, S. B. et al. This observation, for example, was of considerable assistance in the identification of the genes responsible for cystic fibrosis.Below we provide a brief description of human sequence variation, and then describe the strategy and key components of the project. Sequence features in regions of weak and strong linkage disequilibrium.Weir, B.S., Cardon, L.R., Anderson, A.D., Nielsen, D.M., and Hill, W.G. A haplotype map of the human genome.The International HapMap Consortium.
The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. The haplotype map, or "HapMap," is a tool that allows researchers to find genes and genetic variations that affect health and disease.The DNA sequence of any two people is 99.5 percent identical.
The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. The International HapMap Project Web site. The HapMap Web site provides researchers with a number of tools that allow them to analyze the data as well as download data for local analyses. Box 6128, Downtown Station, Montréal, Québec, H3C 3J7, Canada,Department of Anthropology, University of Oklahoma, 455 West Lindsey Street, Norman, Oklahoma, 73019, USA,Vanderbilt University, Center for Genetics and Health Policy, 507 Light Hall, Nashville, Tennessee, 37232, USA,Ellen Wright Clayton, Vivian Ota Wang, Ellen Wright Clayton (co-chair) & Vivian Ota Wang,Wellcome Trust, 183 Euston Road, London, NW1 2BE, UK,Jessica Watkin, Karen Kennedy, Michael G. Dunn, Richard Seabrook, Barbara Skene, John G. Stewart & Patricia Spallone,Washington University School of Medicine, Genome Sequencing Center, Box 8501, 4444 Forest Park Avenue, St Louis, Missouri, 63108, USA,Whitehead Institute/MIT Center for Genome Research, 9 Cambridge Center, Massachusetts, 02142, Cambridge, USA,Chinese Academy of Sciences, 52 Sanlihe Road, Beijing, 100864, China,Chinese Ministry of Science and Technology, 15B Fuxing Road, Beijing, 100862, China,Genome Canada, 150 Metcalfe Street, Suite 2100, Ottawa, Ontario, K2P 1P1, Canada,McGill University, Office of Technology Transfer, 3550 University Street, Montréal, Québec, H3A 2A7, Canada,Génome Québec, 630 Boulevard René-Lévesque Ouest, Montréal, Québec, H3B 1S6, Canada,Ministry of Education, Culture, Sports, Science and Technology, 3-2-2 Kasumigaseki, Chiyodaku, Tokyo, Japan,Hiraki and Associates, Toranomon No. Please enable it to take advantage of the complete set of features!Clipboard, Search History, and several other advanced features are temporarily unavailable.National Center for Biotechnology Information,Unable to load your collection due to an error,Unable to load your delegates due to an error.Nature. The HapMap Web site provides researchers with a number of tools that allow them to analyze the data as well as & Altshuler, D. Quality and completeness of SNP databases.Jeffreys, A. J., Kauppi, L. & Neumann, R. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex.Gabriel, S. B. et al. This observation, for example, was of considerable assistance in the identification of the genes responsible for cystic fibrosis.Below we provide a brief description of human sequence variation, and then describe the strategy and key components of the project. Sequence features in regions of weak and strong linkage disequilibrium.Weir, B.S., Cardon, L.R., Anderson, A.D., Nielsen, D.M., and Hill, W.G. A haplotype map of the human genome.The International HapMap Consortium.
The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. The haplotype map, or "HapMap," is a tool that allows researchers to find genes and genetic variations that affect health and disease.The DNA sequence of any two people is 99.5 percent identical.