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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...
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| Publicat a: | Bioinformatics |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2015
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| Matèries: | |
| Accés en línia: | 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 |
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