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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Detalles Bibliográficos
Autores principales: Keller, Andreas, Harz, Christian, Matzas, Mark, Meder, Benjamin, Katus, Hugo A., Ludwig, Nicole, Fischer, Ulrike, Meese, Eckart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112142/
https://www.ncbi.nlm.nih.gov/pubmed/21695249
http://dx.doi.org/10.1371/journal.pone.0018158

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112142/
https://www.ncbi.nlm.nih.gov/pubmed/21695249
http://dx.doi.org/10.1371/journal.pone.0018158

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