Fig. 1From: Prioritising positively selected variants in whole-genome sequencing data using FineMAVPipeline for calculating the genome-wide FineMAV scores. The boxed region highlighted in grey are the parts of the workflow that are automated by the software. The intermediate output files are deleted when the pipeline is complete. AA: ancestral allele, CADD_PHRED: phred-scaled Combined Annotation Dependent Depletion scores, VEP: Variant Effect Predictor, AF: allele frequency of the alternative alleleBack to article page