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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Keller, Andreas, Harz, Christian, Matzas, Mark, Meder, Benjamin, Katus, Hugo A., Ludwig, Nicole, Fischer, Ulrike, Meese, Eckart
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2011
Konular:
Research Article
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller