Artículo

Global diversity, population stratification, and selection of human copy number variation

Sudmant, Peter H. ; Mallick, Swapan ; Nelson, Bradley J. ; Hormozdiari, Fereydoun ; Krumm, Niklas ; Huddleston, John ; Coe, Bradley P. ; Baker, Carl ; Nordenfelt, Susanne ; Bamshad, Michael ; Jorde, Lynn B. ; Posukh, Olga L. ; Sahakyan, Hovhannes ; Watkins, W. Scott ; Yepiskoposyan, Levon ; Abdullah, M. Syafiq ; Bravi, Claudio Marcelo Icon; Capelli, Cristian ; Hervig, Tor ; Wee, Joseph TS ; Tyler Smith, Chris Icon; George van Driem ; Gallego Romero, Irene ; Jha, Aashish R. ; Karachanak Yankova, Sena ; Toncheva, Draga ; Comas, David ; Henn, Brenna ; Kivisild, Toomas ; Ruiz-Linares, Andres ; Sajantila, Antti ; Metspalu, Ene ; Parik, Jüri ; Villems, Richard ; Starikovskaya, Elena B. ; Ayodo, George ; Beall, Cynthia M. ; Di Rienzo, Anna ; Hammer, Michael ; Khusainova, Rita ; Khusnutdinova, Elza ; Klitz, William ; Winkler, Cheryl ; Labuda, Damian ; Metspalu, Mait ; Tishkoff, Sarah A. ; Dryomov, Stanislav ; Sukernik, Rem ; Patterson, Nick ; Reich, David ; Eichler, Evan E.

Otros responsables

Fecha

08/2015

Editorial

American Association for the Advancement of Science

Revista

Science

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

0036-8075

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

In order to explore the diversity and selective signatures of duplication and deletion human copy number variants (CNVs), we sequenced 236 individuals from 125 distinct human populations. We observed that duplications exhibit fundamentally different population genetic and selective signatures than deletions and are more likely to be stratified between human populations. Through reconstruction of the ancestral human genome, we identify megabases of DNA lost in different human lineages and pinpoint large duplications that introgressed from the extinct Denisova lineage now found at high frequency exclusively in Oceanic populations. We find that the proportion of CNV base pairs to single nucleotide variant base pairs is greater among non-Africans than it is among African populations but we conclude that this difference is likely due to unique aspects of non-African population history as opposed to differences in CNV load.

Aprobación

Revisión

Complementado por

Referenciado por

Licencia Creative Commons

Excepto donde se indique lo contrario, la licencia de este ítem se describe como by-nc-sa