MASSACHUSETTS GENERAL HOSPITAL
A copy number variant discovery pipeline for integrated genome-exome sequencing
A copy number variant discovery pipeline for integrated genome-exome sequencing is a funding opportunity from MASSACHUSETTS GENERAL HOSPITAL, up to 206250, closing August 31, 2027.
Aug 31, 2027
(396d left)Overview
Abstract Copy number variants (CNVs) involve deletions and duplications of genomic segments spanning more than 50 basepairs and represent one of the most penetrant sources of pathogenic variants in neuropsychiatric disorders, with myriad impacts on many other human phenotypes as well. However, the relative impact of…