Fig. 1From: Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing dataFlowchart showing the main steps of our comparison, including preprocessing of the data, detection of copy number variations (CNVs) with six different algorithms (BIC-seq2, Canvas, CNVnator, FREEC, HMMcopy, and QDNAseq) and evaluation and validation of the results. The karyotyping results from the KaryoLiteTM BoBsTM assay are from an earlier study [9]Back to article page