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An approximate Bayesian approach for mapping paired-end DNA reads to a reference genome
Summary: Many high-throughput sequencing experiments produce paired DNA reads. Paired-end DNA reads provide extra positional information that is useful in reliable mapping of short reads to a reference genome, as well as in downstream analyses of structural variations. Given the importance of paired...
Autores principales: | Shrestha, Anish Man Singh, Frith, Martin C. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3624798/ https://www.ncbi.nlm.nih.gov/pubmed/23413433 http://dx.doi.org/10.1093/bioinformatics/btt073 |
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