Fig. 2
From: Prioritising positively selected variants in whole-genome sequencing data using FineMAV
Utilising the chunk size option. A Diagram illustrating how the software separates the input files into chunks and iterates through them when performing the FineMAV calculations. It proceeds to merge them into one output file. B Utilising the chunk size option. A graph that compares the time taken and the maximum random access memory (RAM) when different chunk sizes for a dataset of 66,236,516 biallelic SNPs is used