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Computational methods and resources for the interpretation of genomic variants in cancer
The recent improvement of the high-throughput sequencing technologies is having a strong impact on the detection of genetic variations associated with cancer. Several institutions worldwide have been sequencing the whole exomes and or genomes of cancer patients in the thousands, thereby providing an...
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| Vydáno v: | BMC Genomics |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4480958/ https://ncbi.nlm.nih.gov/pubmed/26111056 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-16-S8-S7 |
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