Prioritizing Clinically Relevant Copy Number Variation from Genetic Interactions and Gene Function Data.

It is becoming increasingly necessary to develop computerized methods for identifying the few disease-causing variants from hundreds discovered in each individual patient. This problem is especially relevant for Copy Number Variants (CNVs), which can be cheaply interrogated via low-cost hybridizatio...

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Bibliographic Details
Main Authors: Justin Foong, Marta Girdea, James Stavropoulos, Michael Brudno
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4593641?pdf=render

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