Prioritising positively selected variants in whole-genome sequencing data using FineMAV.
Wahyudi F, Aghakhanian F, Rahman S, Teo YY, Szpak M, Dhaliwal J, Ayub Q.
Wahyudi F, et al.
BMC Bioinformatics. 2021 Dec 18;22(1):604. doi: 10.1186/s12859-021-04506-9.
BMC Bioinformatics. 2021.
PMID: 34922440
Free PMC article.
The software tool is publicly available at https://github.com/fadilla-wahyudi/finemav . CONCLUSIONS: The software tool described here determines genome-wide FineMAV scores, using low or high-coverage whole-genome sequencing datasets, that can be used to prioritize a list o …
The software tool is publicly available at https://github.com/fadilla-wahyudi/finemav . CONCLUSIONS: The software tool described here …