Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Laurens van de Wiel"'
Autor:
Hector Mendez, Devon Bonner, Chloe Reuter, Jennefer Kohler, Shruti Marwaha, Laurens van de Wiel, Elijah Kravets, Charlotte Ostrow, Raquel Alvarez, Sara Emami, Meghan Halley, Holly Tabor, Suha Bachir, Jonathan Bernstein, Matthew Wheeler
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101545- (2024)
Externí odkaz:
https://doaj.org/article/ba56d5132efc42ef8a6836193f611fd2
Autor:
Taibo Li, Nicole Ferraro, Benjamin J. Strober, Francois Aguet, Silva Kasela, Marios Arvanitis, Bohan Ni, Laurens van de Wiel, Elliot Hershberg, Kristin Ardlie, Dan E. Arking, Rebecca L. Beer, Jennifer Brody, Thomas W Blackwell, Clary Clish, Stacey Gabriel, Robert Gerszten, Xiuqing Guo, Namrata Gupta, W. Craig Johnson, Tuuli Lappalainen, Henry J. Lin, Yongmei Liu, Deborah A. Nickerson, George Papanicolaou, Jonathan K. Pritchard, Pankaj Qasba, Ali Shojaie, Josh Smith, Nona Sotoodehnia, Kent D. Taylor, Russell P. Tracy, David Van Den Berg, Matthew Wheeler, Stephen S. Rich, Jerome I. Rotter, Alexis Battle, Stephen B. Montgomery
Each human genome has tens of thousands of rare genetic variants; however, identifying impactful rare variants remains a major challenge. We demonstrate how use of personal multi-omics can enable identification of impactful rare variants by using the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c050eac8cfa187ab887edb7d00a4e3dd
https://doi.org/10.1101/2022.09.07.507008
https://doi.org/10.1101/2022.09.07.507008
