Cargando...
PVAAS: identify variants associated with aberrant splicing from RNA-seq
Motivation: RNA-seq has been widely used to study the transcriptome. Comparing to microarray, sequencing-based RNA-seq is able to identify splicing variants and single nucleotide variants in one experiment simultaneously. This provides unique opportunity to detect variants that associated with aberr...
Gardado en:
| Publicado en: | Bioinformatics |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2015
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4807355/ https://ncbi.nlm.nih.gov/pubmed/25573917 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv001 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|