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
scientific article published on 23 December 2019
Author/s
author: Madeline H Kowalski, Huijun Qian, Jonathan D Rosen, Amanda L Tapia, Maria Argos, Donna K Arnett, Stephanie A Bien, Donald W Bowden, Steven Buyske, Jianwen Cai, Hélène Choquet, Mariaelisa Graff, Susan R Heckbert, Tanika N Kelly, Ruth J. Loos, Steven A Lubitz, Caitlin P McHugh, Jee-Young Moon, Nicholette D Palmer, Patricia A Peyser, Jerome I Rotter, Jennifer A Smith, Kent D Taylor, Timothy A Thornton, Tao Wang, Scott T Weiss, Kerri L Wiggins, James G. Wilson, Lisa R Yanek, Laura Raffield, Alexander P Reiner, Yun Li, NHLBI Trans-Omics for Precision Medicine Consortium, Kari E North, John Blangero, Sharon L R Kardia, L. Adrienne Cupples, Patrick T Ellinor, Georgios Papanikolaou, Edwin K Silverman, Michael H Cho, Russell P Tracy, Stephen S Rich, Alanna Morrison, Kathleen C Barnes, Joshua C Bis, Marguerite R Irvin, Courtney G Montgomery, Paul L Auer, Bertha A Hidalgo, Michelle Daya, Jessica Lasky-Su, Seung-Hoan Choi, Charles Kooperberg, Jean-Paul P.M. de Vries, Eric Boerwinkle, Christy L Avery, Namrata Gupta, Ziyi Hou, Lewis Becker, Nauder Faraday, Stacey Gabriel, Santhi K Ganesh, Chani J Hodonsky, Eric Jorgenson, Rasika A Mathias, Nathan Pankratz, Myriam Fornage, Andrew D. Johnson
Work details
Copyright status
Copyright status information is not available for this work. The copyright status depends on the jurisdiction, the author's date of death and the date the work was created or published.
To learn more about copyright terms in different countries, visit the countries and terms page.