Additional file 5: of GenESysV: a fast, intuitive and scalable genome exploration open source tool for variants generated from high-throughput sequencing projects

Figure S2. VCF data importing times for input files with a fixed number of samples but an increasing number of variants. The VEP annotated 1000 Genomes Project Phase3 VCF file is used as input to create a series of VCF files to include the first 10, 20, 30, 40, 50, 60 and 70 million variants. These files (including the full VCF file containing the 85 million variants) are used as inputs for benchmarking data importation. See Additional file 9 for details. (TIFF 9492 kb)