A carregar...
RASER: reads aligner for SNPs and editing sites of RNA
Motivation: Accurate identification of genetic variants such as single-nucleotide polymorphisms (SNPs) or RNA editing sites from RNA-Seq reads is important, yet challenging, because it necessitates a very low false-positive rate in read mapping. Although many read aligners are available, no single a...
Na minha lista:
| Publicado no: | Bioinformatics |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4692970/ https://ncbi.nlm.nih.gov/pubmed/26323713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv505 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|