Identification of novel SNPs in glioblastoma using targeted resequencing.

High-throughput sequencing opens avenues to find genetic variations that may be indicative of an increased risk for certain diseases. Linking these genomic data to other "omics" approaches bears the potential to deepen our understanding of pathogenic processes at the molecular level. To de...

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Bibliographic Details
Main Authors: Andreas Keller, Christian Harz, Mark Matzas, Benjamin Meder, Hugo A Katus, Nicole Ludwig, Ulrike Fischer, Eckart Meese
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3112142?pdf=render