Fig. 2From: Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platformsEvaluation of CNVs from 50 datasets on two benchmarks. Dot plot shows the sensitivity and precision of CNVs on ten datasets using five tools compared with those using Benchmark1 (left) and Benchmark2 (right). Ten datasets are marked with different colours, and five tools are marked with different point types. Benchmark1, data by Ryan et al. 2014; Benchmark2, data by Peter et al. 2015Back to article page