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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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| Опубликовано в: : | BMC Med Inform Decis Mak |
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| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2019
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| Предметы: | |
| Online-ссылка: | 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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