Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans

por Haraksingh, Rajini R., Abyzov, Alexej, Urban, Alexander Eckehart
Publicado 2017

Genome-Wide Mapping of Copy Number Variation in Humans: Comparative Analysis of High Resolution Array Platforms

por Haraksingh, Rajini R., Abyzov, Alexej, Gerstein, Mark, Urban, Alexander E., Snyder, Michael
Publicado 2011

Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss

por Haraksingh, Rajini R, Jahanbani, Fereshteh, Rodriguez-Paris, Juan, Gelernter, Joel, Nadeau, Kari C, Oghalai, John S, Schrijver, Iris, Snyder, Michael P
Publicado 2014

Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562

por Zhou, Bo, Ho, Steve S., Greer, Stephanie U., Zhu, Xiaowei, Bell, John M., Arthur, Joseph G., Spies, Noah, Zhang, Xianglong, Byeon, Seunggyu, Pattni, Reenal, Ben-Efraim, Noa, Haney, Michael S., Haraksingh, Rajini R., Song, Giltae, Ji, Hanlee P., Perrin, Dimitri, Wong, Wing H., Abyzov, Alexej, Urban, Alexander E.
Publicado 2019