Cleaning clinical genomic data: Simple identification and removal of recurrently miscalled variants in single genomes
Matthew A. Field, Gaétan Burgio, Jalila Al Shekaili, Simon J. Foote, Matthew Cook, T. Daniel Andrews
The paper identifies and removes recurrent false positive variants in single genomes to improve the accuracy of variant calling.
bioRxiv · Dec 20, 2017 · PreprintGenomics