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Acceleration of short and long DNA read mapping without loss of accuracy using suffix array
HPG Aligner applies suffix arrays for DNA read mapping. This implementation produces a highly sensitive and extremely fast mapping of DNA reads that scales up almost linearly with read length. The approach presented here is faster (over 20× for long reads) and more sensitive (over 98% in a wide rang...
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| Publicat a: | Bioinformatics |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4816028/ https://ncbi.nlm.nih.gov/pubmed/25143289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu553 |
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