Učitavanje...
Expanding the computational toolbox for mining cancer genomes
High-throughput DNA sequencing has revolutionized cancer genomics with numerous discoveries relevant to cancer diagnosis and treatment. The latest sequencing and analysis methods have successfully identified somatic alterations including single nucleotide variants (SNVs), insertions and deletions (i...
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| Glavni autori: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4168012/ https://ncbi.nlm.nih.gov/pubmed/25001846 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nrg3767 |
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