Skip to main content
Fig. 5 | BMC Genomics

Fig. 5

From: Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data

Fig. 5

Performance evaluation of the six algorithms using the cell line data with the criteria of ≥ 50 % overlap and no minimum length requirement for the detected CNVs. a, d True positive rate (TPR), b, e False discovery rate (FDR), and c, f F1 score of the CNV detections. The red and blue dots depict the abnormal and normal samples, respectively

Back to article page