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Population-wide copy number variation calling using variant call format files from 6,898 individuals.

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第一作者： Grace,Png

第一单位： Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.;Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.;Institute of Translational Genomics, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany.

作者： Grace,Png ^[1] ; Daniel,Suveges ^[2] ; Young-Chan,Park ^[3] ; Klaudia,Walter ^[4] ; Kousik,Kundu ^[4] ; Ioanna,Ntalla ^[5] ; Emmanouil,Tsafantakis ^[6] ; Maria,Karaleftheri ^[7] ; George,Dedoussis ^[8] ; Eleftheria,Zeggini ^[9] ; Arthur,Gilly ^[10]

作者单位： Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.;Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.;Institute of Translational Genomics, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany. ^[1] Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.;European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, United Kingdom. ^[2] Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.;Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom. ^[3] Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom. ^[4] William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom. ^[5] Anogia Medical Centre, Anogia, Greece. ^[6] Echinos Medical Centre, Echinos, Greece. ^[7] Department of Nutrition and Dietetics, School of Health Science and Education, Harokopio University of Athens, Athens, Greece. ^[8] Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.;Institute of Translational Genomics, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany. ^[9] Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.;Institute of Translational Genomics, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany.;Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom. ^[10]

关键词 association study copy-number variant whole-genome sequencing