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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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| Publicado no: | Gigascience |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4989487/ https://ncbi.nlm.nih.gov/pubmed/27538485 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13742-016-0143-4 |
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