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Very low-depth whole-genome sequencing in complex trait association studies.

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第一作者： Arthur,Gilly

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

作者： Arthur,Gilly ^[1] ; Lorraine,Southam ^[2] ; Daniel,Suveges ^[3] ; Karoline,Kuchenbaecker ^[3] ; Rachel,Moore ^[3] ; Giorgio E M,Melloni ^[4] ; Konstantinos,Hatzikotoulas ^[1] ; Aliki-Eleni,Farmaki ^[5] ; Graham,Ritchie ^[6] ; Jeremy,Schwartzentruber ^[3] ; Petr,Danecek ^[3] ; Britt,Kilian ^[3] ; Martin O,Pollard ^[3] ; Xiangyu,Ge ^[3] ; Emmanouil,Tsafantakis ^[7] ; George,Dedoussis ^[5] ; Eleftheria,Zeggini ^[1]

作者单位： Department of Human Genetics, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.;Institute of Translational Genomics, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany. ^[1] Department of Human Genetics, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.;Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK. ^[2] Department of Human Genetics, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. ^[3] Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. ^[4] Department of Nutrition and Dietetics, School of Health Science and Education, Harokopio University of Athens, Athens, Greece. ^[5] Department of Human Genetics, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.;European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, UK. ^[6] Anogia Medical Centre, Anogia, Greece. ^[7]

医学主题词基因型(Genotype);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);多因子遗传(Multifactorial Inheritance);多态性, 单核苷酸(Polymorphism, Single Nucleotide)

DOI 10.1093/bioinformatics/bty1032

PMID 30576415

发布时间 2025-05-30

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