Fast read alignment with incorporation of known genomic variants
Abstract 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 sequen...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2019-12-01
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| coleção: | BMC Medical Informatics and Decision Making |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.1186/s12911-019-0960-3 |
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