RES-Scanner: a software package for genome-wide identification of RNA-editing sites

BACKGROUND: High-throughput sequencing (HTS) provides a powerful solution for the genome-wide identification of RNA-editing sites. However, it remains a great challenge to distinguish RNA-editing sites from genetic variants and technical artifacts caused by sequencing or read-mapping errors. RESULTS...

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Detalles Bibliográficos
Autores principales: Wang, Zongji, Lian, Jinmin, Li, Qiye, Zhang, Pei, Zhou, Yang, Zhan, Xiaoyu, Zhang, Guojie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Technical Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989487/
https://www.ncbi.nlm.nih.gov/pubmed/27538485
http://dx.doi.org/10.1186/s13742-016-0143-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989487/
https://www.ncbi.nlm.nih.gov/pubmed/27538485
http://dx.doi.org/10.1186/s13742-016-0143-4

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