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

by Haraksingh, Rajini R., Abyzov, Alexej, Gerstein, Mark, Urban, Alexander E., Snyder, Michael
Published 2011

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

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