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