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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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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2011
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| Assuntos: | |
| Acesso em linha: | 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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