A carregar...

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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:BMC Bioinformatics
Main Authors: Quaglieri, Anna, Flensburg, Christoffer, Speed, Terence P., Majewski, Ian J.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!