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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 detect novel...

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Bibliografiske detaljer
Main Authors: Keller, Andreas, Harz, Christian, Matzas, Mark, Meder, Benjamin, Katus, Hugo A., Ludwig, Nicole, Fischer, Ulrike, Meese, Eckart
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2011
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3112142/
https://ncbi.nlm.nih.gov/pubmed/21695249
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0018158
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