nf-core/isoseq: simple gene and isoform annotation with PacBio Iso-Seq long-read sequencing.
Bioinformatics
; 39(5)2023 05 04.
Article
em En
| MEDLINE
| ID: mdl-36961337
ABSTRACT
MOTIVATION Iso-Seq RNA long-read sequencing enables the identification of full-length transcripts and isoforms, removing the need for complex analysis such as transcriptome assembly. However, the raw sequencing data need to be processed in a series of steps before annotation is complete. Here, we present nf-core/isoseq, a pipeline for automatic read processing and genome annotation. Following nf-core guidelines, the pipeline has few dependencies and can be run on any of platforms. AVAILABILITY AND IMPLEMENTATION The pipeline is freely available online on the nf-core website (https//nf-co.re/isoseq) and on GitHub (https//github.com/nf-core/isoseq) under MIT License (DOI 10.5281/zenodo.7116979).
Texto completo:
1
Bases de dados:
MEDLINE
Assunto principal:
Genoma
/
Processamento Alternativo
Idioma:
En
Revista:
Bioinformatics
Assunto da revista:
INFORMATICA MEDICA
Ano de publicação:
2023
Tipo de documento:
Article
País de afiliação:
Reino Unido