Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Daniel Taliun , Daniel Harris , Michael D. Kessler , Daniel Taliun , Daniel Harris , Michael D. Kessler , Jedidiah Carlson , Zachary A. Szpiech , Raúl Torres , Sarah A. Gagliano Taliun , André Corvelo , Stephanie M. Gogarten , Hyun Min Kang , Achilleas Pitsillides , Jonathon LeFaive , Seung‐been Lee , Xiaowen Tian , Brian L. Browning , Sayantan Das , Anne‐Katrin Emde , Wayne E. Clarke , Douglas P. Loesch , Amol C. Shetty , Thomas W. Blackwell , Albert V. Smith , Quenna Wong , Xiaoming Liu , Matthew P. Conomos , Dean Bobo , François Aguet , Christine M. Albert , Álvaro Alonso , Kristin Ardlie , Dan E. Arking , Stella Aslibekyan , Paul L. Auer , John Barnard , R. Graham Barr , Lucas Barwick , Lewis C. Becker , Rebecca Beer , Emelia J. Benjamin , Lawrence F. Bielak , John Blangero , Michael Boehnke , Donald W. Bowden , Jennifer A. Brody , Esteban G. Burchard , Brian E. Cade , James F. Casella , Brandon Chalazan , Daniel I. Chasman , Yii‐Der Ida Chen , Michael H. Cho , Seung Hoan Choi , Mina K. Chung , Clary B. Clish , Adolfo Correa , Joanne E. Curran , Brian Custer , Dawood Darbar , Michelle Daya , Mariza de Andrade , Dawn L. DeMeo , Susan K. Dutcher , Patrick T. Ellinor , Leslie S. Emery , Celeste Eng , Diane Fatkin , Tasha E. Fingerlin , Lukas Forer , Myriam Fornage , Nora Franceschini , Christian Fuchsberger , Stephanie M. Fullerton , Søren Germer , Mark T. Gladwin , Daniel J. Gottlieb , Xiuqing Guo , Michael E. Hall , Jiang He , Nancy L. Heard‐Costa , Susan R. Heckbert , Marguerite R. Irvin , Jill M. Johnsen , Andrew D. Johnson , Robert C. Kaplan , Sharon L. R. Kardia , Tanika N. Kelly , Shannon Kelly , Eimear E. Kenny , Douglas P. Kiel , Robert Klemmer , Barbara A. Konkle , Charles Kooperberg , Anna Köttgen , Leslie A. Lange , Jessica Lasky‐Su , Daniel Levy , Xihong Lin , Keng‐Han Lin , Chunyu Liu , Ruth J. F. Loos
2021 Nature 2,076 citations

Keywords

Imputation (statistics)Biology1000 Genomes ProjectGeneticsGenomeHaplotypeGenomicsWhole genome sequencingDNA sequencingStructural variationCopy-number variationComputational biologyGenetic variationPrecision medicineHuman geneticsPhenotypeGenome-wide association studySingle-nucleotide polymorphismGenotypeGeneMissing dataComputer science

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Year
2021
Type
article
Volume
590
Issue
7845
Pages
290-299
Citations
2076
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Daniel Taliun, Daniel Harris, Michael D. Kessler et al. (2021). Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature , 590 (7845) , 290-299. https://doi.org/10.1038/s41586-021-03205-y

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DOI
10.1038/s41586-021-03205-y