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RandAL: a randomized approach to aligning DNA sequences to reference genomes
BACKGROUND: The alignment of short reads generated by next-generation sequencers to genomes is an important problem in many biomedical and bioinformatics applications. Although many proposed methods work very well on narrow ranges of read lengths, they tend to suffer in performance and alignment qua...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120144/ https://www.ncbi.nlm.nih.gov/pubmed/25081493 http://dx.doi.org/10.1186/1471-2164-15-S5-S2 |