A global reference for human genetic variation.

Added 1885 days ago (04.10.2015)
Authors: 1000 Genomes Project Consortium, Corresponding authors, Steering committee, Production group, Baylor College of Medicine, BGI-Shenzhen, Broad Institute of MIT and Harvard, Coriell Institute for Medical Research, European Molecular Biology Laboratory, European Bioinformatics Institute, Illumina, Max Planck Institute for Molecular Genetics, McDonnell Genome Institute at Washington University, US National Institutes of Health, University of Oxford, Wellcome Trust Sanger Institute, Analysis group, Affymetrix, Albert Einstein College of Medicine, Baylor College of Medicine, BGI-Shenzhen, Bilkent University, Boston College, Broad Institute of MIT and Harvard, Cold Spring Harbor Laboratory, Cornell University, European Molecular Biology Laboratory, European Molecular Biology Laboratory, European Bioinformatics Institute, Harvard University, Human Gene Mutation Database, Illumina, Icahn School of Medicine at Mount Sinai, Louisiana State University, Massachusetts General Hospital, Max Planck Institute for Molecular Genetics, McDonnell Genome Institute at Washington University, McGill University, National Eye Institute, NIH, New York Genome Center, Ontario Institute for Cancer Research, Pennsylvania State University, Rutgers Cancer Institute of New Jersey, Stanford University, Tel-Aviv University, Jackson Laboratory for Genomic Medicine, Thermo Fisher Scientific, Translational Genomics Research Institute, US National Institutes of Health, University of California, San Diego, University of California, San Francisco, University of California, Santa Cruz, University of Chicago, University College London, University of Geneva, University of Maryland School of Medicine, University of Michigan, University of Montréal, University of North Carolina at Chapel Hill, University of North Carolina at Charlotte, University of Oxford, University of Puerto Rico, University of Texas Health Sciences Center at Houston, University of Utah, University of Washington, Weill Cornell Medical College, Wellcome Trust Sanger Institute, Yale University, Structural variation group, BGI-Shenzhen, Bilkent University, Boston College, Broad Institute of MIT and Harvard, Cold Spring Harbor Laboratory, Cornell University, European Molecular Biology Laboratory, European Molecular Biology Laboratory, European Bioinformatics Institute, Illumina, Leiden University Medical Center, Louisiana State University, McDonnell Genome Institute at Washington University, Stanford University, Jackson Laboratory for Genomic Medicine, Translational Genomics Research Institute, US National Institutes of Health, University of California, San Diego, University of Maryland School of Medicine, University of Michigan, University of North Carolina at Charlotte, University of Oxford, University of Texas MD Anderson Cancer Center, University of Utah, University of Washington, Vanderbilt University School of Medicine, Weill Cornell Medical College, Wellcome Trust Sanger Institute, Yale University, Exome group, Baylor College of Medicine, BGI-Shenzhen, Boston College, Broad Institute of MIT and Harvard, Cornell University, European Molecular Biology Laboratory, European Bioinformatics Institute, Massachusetts General Hospital, McDonnell Genome Institute at Washington University, McGill University, Stanford University, Translational Genomics Research Institute, US National Institutes of Health, University of Geneva, University of Michigan, University of Oxford, Yale University, Functional interpretation group, Cornell University, European Molecular Biology Laboratory, European Bioinformatics Institute, Harvard University, Stanford University, Weill Cornell Medical College, Wellcome Trust Sanger Institute, Yale University, Chromosome Y group, Albert Einstein College of Medicine, American Museum of Natural History, Arizona State University, Boston College, Broad Institute of MIT and Harvard, Cornell University, European Molecular Biology Laboratory, European Bioinformatics Institute, New York Genome Center, Stanford University, Jackson Laboratory for Genomic Medicine, University of Michigan, University of Queensland, Virginia Bioinformatics Institute, Wellcome Trust Sanger Institute, Data coordination center group, Baylor College of Medicine, BGI-Shenzhen, Broad Institute of MIT and Harvard, European Molecular Biology Laboratory, European Bioinformatics Institute, Illumina, Max Planck Institute for Molecular Genetics, McDonnell Genome Institute at Washington University, Translational Genomics Research Institute, US National Institutes of Health, University of California, Santa Cruz, University of Michigan, University of Oxford, Wellcome Trust Sanger Institute, Samples and ELSI group, Sample collection, British fromEngland and Scotland (GBR), Colombians in Medellín, Colombia (CLM), Han Chinese South (CHS), Finnish in Finland (FIN), Iberian Populations in Spain (IBS), Puerto Ricans in Puerto Rico (PUR), African Caribbean in Barbados (ACB), Bengali in Bangladesh (BEB), Chinese Dai in Xishuangbanna, China (CDX),Esan in Nigeria (ESN), Gambian in Western Division – Mandinka (GWD), Indian Telugu in the UK (ITU) and Sri Lankan Tamil in the UK (STU), Kinh in Ho Chi Minh City, Vietnam (KHV), Mende in Sierra Leone (MSL), Peruvian in Lima, Peru (PEL), Punjabi in Lahore, Pakistan (PJL), Scientific management, Writing group, European Molecular Biology Laboratory European Bioinformatics Institute, National Eye Institute NIH, University of California San Diego, University of California San Francisco, University of California Santa Cruz, British from England and Scotland GBR, Colombians in Medellín Colombia CLM, Han Chinese South CHS, Finnish in Finland FIN, Iberian Populations in Spain IBS, Puerto Ricans in Puerto Rico PUR, African Caribbean in Barbados ACB, Bengali in Bangladesh BEB, Chinese Dai in Xishuangbanna China CDX, Esan in Nigeria ESN, Gambian in Western Division - Mandinka GWD, Indian Teluguin the UK ITU and Sri Lankan Tamil in the UK STU, Kinh in Ho Chi Minh City Vietnam KHV, Mende in Sierra Leone MSL, Peruvian in Lima Peru PEL, Punjabi in Lahore Pakistan PJL
PubMed id: 26432245
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