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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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| Publicado no: | BMC Med Inform Decis Mak |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | 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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