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Fast and SNP-tolerant detection of complex variants and splicing in short reads
Motivation: Next-generation sequencing captures sequence differences in reads relative to a reference genome or transcriptome, including splicing events and complex variants involving multiple mismatches and long indels. We present computational methods for fast detection of complex variants and spl...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2844994/ https://www.ncbi.nlm.nih.gov/pubmed/20147302 http://dx.doi.org/10.1093/bioinformatics/btq057 |