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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Detalles Bibliográficos
Autores principales: Guo, Hongzhe, Liu, Bo, Guan, Dengfeng, Fu, Yilei, Wang, Yadong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921400/
https://www.ncbi.nlm.nih.gov/pubmed/31856811
http://dx.doi.org/10.1186/s12911-019-0960-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921400/
https://www.ncbi.nlm.nih.gov/pubmed/31856811
http://dx.doi.org/10.1186/s12911-019-0960-3

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