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...

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Detalles Bibliográficos
Autores principales: Vo, Nam S, Tran, Quang, Niraula, Nobal, Phan, Vinhthuy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
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

Internet

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

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