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Joint genotype inference with germline and somatic mutations
The joint sequencing of related genomes has become an important means to discover rare variants. Normal-tumor genome pairs are routinely sequenced together to find somatic mutations and their associations with different cancers. Parental and sibling genomes reveal de novo germline mutations and inhe...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3622648/ https://ncbi.nlm.nih.gov/pubmed/23734724 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-S5-S3 |
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