Finding functional disease-associated non-coding variation using next-generation sequencing
Paolo Devanna, Xiaowei Sylvia Chen, Joses Ho, Dario Gajewski, Alessandro Gialluisi, Clyde Francks, Simon E Fisher, Dianne F Newbury, Sonja C Vernes
The paper identifies a non-coding variant in a microRNA binding site associated with language impairment using whole exome sequencing data from a cohort of children.
bioRxiv · Jun 22, 2016Genetics