Skip to main content
Fig. 2 | BMC Bioinformatics

Fig. 2

From: SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data

Fig. 2

An example of simulated CNV data on chromosome 1. The data set, computationally simulated, includes two deletions and two duplications at each of four lengths. Black dots represent read density over 500 bp fixed windows along the entire chromosome. The red bands indicate the results of SeqCNV analysis. Horizontal lines mark significant points of deletion or gain

Back to article page