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Sensitive and fast mapping of di-base encoded reads
Motivation: Discovering variation among high-throughput sequenced genomes relies on efficient and effective mapping of sequence reads. The speed, sensitivity and accuracy of read mapping are crucial to determining the full spectrum of single nucleotide variants (SNVs) as well as structural variants...
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| Main Authors: | , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Oxford University Press
2011
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3129524/ https://ncbi.nlm.nih.gov/pubmed/21586516 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr303 |
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