Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations | Zendy

M.H. Kowalski | Zendy; H. Qian | Zendy; Zi-Xuan Hou | Zendy; J.D. Rosen | Zendy; A.L. Tapia | Zendy; Yongtao Shan | Zendy; D. Jain | Zendy; M. Argos | Zendy; D.K. Arnett | Zendy; Christy L. Avery | Zendy; K.C. Barnes | Zendy; L.C. Becker | Zendy; S.A. Bien | Zendy; J.C. Bis | Zendy; J. Blangero | Zendy; E. Boerwinkle | Zendy; D.W. Bowden | Zendy; S. Buyske | Zendy; J. Cai | Zendy; M.H. Cho | Zendy; S.H. Choi | Zendy; H. Choquet | Zendy; L. A. Cupples | Zendy; M. Cushman | Zendy; M. Daya | Zendy; P.S. de Vries | Zendy; P.T. Ellinor | Zendy; N. Faraday | Zendy; M. Fornage | Zendy; S. Gabriel | Zendy; Sruthi Ganesh | Zendy; M. Graff | Zendy; N. Gupta | Zendy; Jesse He | Zendy; S.R. Heckbert | Zendy; B. Hidalgo | Zendy; Chani J. Hodonsky | Zendy; M.R. Irvin | Zendy; A.D. Johnson | Zendy; E. Jorgenson | Zendy; Rob Kaplan | Zendy; S.L.R. Kardia | Zendy; T.N. Kelly | Zendy; C. Kooperberg | Zendy; J.A. Lasky-Su | Zendy; R.J.F. Loos | Zendy; S.A. Lubitz | Zendy; R.A. Mathias | Zendy; C.P. McHugh | Zendy; C. Montgomery | Zendy; J.-Y. Moon | Zendy; Alanna C. Morrison | Zendy; N.D. Palmer | Zendy; N. Pankratz | Zendy; G.J. Papanicolaou | Zendy; J.M. Peralta | Zendy; P.A. Peyser | Zendy; S.S. Rich | Zendy; J.I. Rotter | Zendy; E.K. Silverman | Zendy; J.A. Smith | Zendy; N.L. Smith | Zendy; K.D. Taylor | Zendy; T.A. Thornton | Zendy; H.K. Tiwari | Zendy; R.P. Tracy | Zendy; T. Wang | Zendy; S.T. Weiss | Zendy; L.-C. Weng | Zendy; K.L. Wiggins | Zendy; J.G. Wilson | Zendy; L.R. Yanek | Zendy; S. Zöllner | Zendy; K.E. North | Zendy; Paul L. Auer | Zendy; NHLBI Trans-Omics for Precision Medicine Consortium | Zendy; TOPMed Hematology Hemostasis Working Group | Zendy; Laura M. Raffield | Zendy; A.P. Reiner | Zendy; Y. Li | Zendy

Open Access

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

Author(s) -

M.H. Kowalski,

H. Qian,

Zi-Xuan Hou,

J.D. Rosen,

A.L. Tapia,

Yongtao Shan,

D. Jain,

M. Argos,

D.K. Arnett,

Christy L. Avery,

K.C. Barnes,

L.C. Becker,

S.A. Bien,

J.C. Bis,

J. Blangero,

E. Boerwinkle,

D.W. Bowden,

S. Buyske,

J. Cai,

M.H. Cho,

S.H. Choi,

H. Choquet,

L. A. Cupples,

M. Cushman,

M. Daya,

P.S. de Vries,

P.T. Ellinor,

N. Faraday,

M. Fornage,

S. Gabriel,

Sruthi Ganesh,

M. Graff,

N. Gupta,

Jesse He,

S.R. Heckbert,

B. Hidalgo,

Chani J. Hodonsky,

M.R. Irvin,

A.D. Johnson,

E. Jorgenson,

Rob Kaplan,

S.L.R. Kardia,

T.N. Kelly,

C. Kooperberg,

J.A. Lasky-Su,

R.J.F. Loos,

S.A. Lubitz,

R.A. Mathias,

C.P. McHugh,

C. Montgomery,

J.-Y. Moon,

Alanna C. Morrison,

N.D. Palmer,

N. Pankratz,

G.J. Papanicolaou,

J.M. Peralta,

P.A. Peyser,

S.S. Rich,

J.I. Rotter,

E.K. Silverman,

J.A. Smith,

N.L. Smith,

K.D. Taylor,

T.A. Thornton,

H.K. Tiwari,

R.P. Tracy,

T. Wang,

S.T. Weiss,

L.-C. Weng,

K.L. Wiggins,

J.G. Wilson,

L.R. Yanek,

S. Zöllner,

K.E. North,

Paul L. Auer,

NHLBI Trans-Omics for Precision Medicine Consortium,

TOPMed Hematology Hemostasis Working Group,

Laura M. Raffield,

A.P. Reiner,

Y. Li

Publication year - 2019

Publication title -

carolina digital repository (university of north carolina at chapel hill)

Language(s) - English

DOI - 10.17615/e6ew-j192

Subject(s) - imputation (statistics) , genome wide association study , african american , precision medicine , computational biology , genetics , medicine , biology , single nucleotide polymorphism , gene , computer science , genotype , missing data , machine learning , history , ethnology

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