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Finding a suitable library size to call variants in RNA-Seq
BACKGROUND: RNA sequencing allows the study of both gene expression changes and transcribed mutations, providing a highly effective way to gain insight into cancer biology. When planning the sequencing of a large cohort of samples, library size is a fundamental factor affecting both the overall cost...
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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7708150/ https://ncbi.nlm.nih.gov/pubmed/33261552 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-020-03860-4 |
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