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Comparison of somatic mutation calling methods in amplicon and whole exome sequence data
BACKGROUND: High-throughput sequencing is rapidly becoming common practice in clinical diagnosis and cancer research. Many algorithms have been developed for somatic single nucleotide variant (SNV) detection in matched tumor-normal DNA sequencing. Although numerous studies have compared the performa...
Gorde:
| Egile Nagusiak: | , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3986649/ https://ncbi.nlm.nih.gov/pubmed/24678773 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-244 |
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