Fig. 1From: FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods1000GP 27 sample study. 27 samples were selected from the 2504 samples used in the 1000GP due to the availability of high-quality, 50X sequencing coverage comprising polymerase chain reaction-free, 250 bp Illumina PE reads (ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20130502/supporting/high_coverage_alignments/20141118_high_coverage.alignment.index). SV types represented in the VCF files were deletions, duplications, and inversions while translocations and other complex SVs were excluded. Mean mapping quality > 30 is considered good. %reference refers to what percentage of the reads mapped to the reference genomeBack to article page