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Detection and benchmarking of somatic mutations in cancer genomes using RNA-seq data
To detect functional somatic mutations in tumor samples, whole-exome sequencing (WES) is often used for its reliability and relative low cost. RNA-seq, while generally used to measure gene expression, can potentially also be used for identification of somatic mutations. However there has been little...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
PeerJ Inc.
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074801/ https://www.ncbi.nlm.nih.gov/pubmed/30083469 http://dx.doi.org/10.7717/peerj.5362 |