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FunSeq2: a framework for prioritizing noncoding regulatory variants in cancer
Identification of noncoding drivers from thousands of somatic alterations in a typical tumor is a difficult and unsolved problem. We report a computational framework, FunSeq2, to annotate and prioritize these mutations. The framework combines an adjustable data context integrating large-scale genomi...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4203974/ https://ncbi.nlm.nih.gov/pubmed/25273974 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-014-0480-5 |
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