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Detecting somatic point mutations in cancer genome sequencing data: a comparison of mutation callers
BACKGROUND: Driven by high throughput next generation sequencing technologies and the pressing need to decipher cancer genomes, computational approaches for detecting somatic single nucleotide variants (sSNVs) have undergone dramatic improvements during the past 2 years. The recently developed tools...
Tallennettuna:
| Päätekijät: | , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3971343/ https://ncbi.nlm.nih.gov/pubmed/24112718 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm495 |
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