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Fast read alignment with incorporation of known genomic variants
BACKGROUND: Many genetic variants have been reported from sequencing projects due to decreasing experimental costs. Compared to the current typical paradigm, read mapping incorporating existing variants can improve the performance of subsequent analysis. This method is supposed to map sequencing rea...
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| Publié dans: | BMC Med Inform Decis Mak |
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| Auteurs principaux: | , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6921400/ https://ncbi.nlm.nih.gov/pubmed/31856811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12911-019-0960-3 |
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