Fig. 5From: CNVind: an open source cloud-based pipeline for rare CNVs detection in whole exome sequencing data based on the depth of coverageEffect of the size of the set of sequencing regions which models background on the results’ sensitivity and precision. a, b relate to the selection of the k most correlated sequencing regions, c, d k random sequencing regions. Additionally, b, d the improvement of individual results relative to the baseline, i.e. all sequencing regions are normalized simultaneously. It is worth paying attention to the fact that reducing the value of k in the knn algorithm to a value equal to 100 (b) allowed for a 3-fold improvement in precision while maintaining a constant level of sensitivity for rare CNVsBack to article page