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Fig. 2 | BMC Genomics

Fig. 2

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

Fig. 2

Genomic map visualization of the copy number variations (CNVs) detected in the simulated dataset using the six algorithms (rows 1–6) along with the ground truth CNVs (row 7) in the respective chromosomal locations. Deletions are marked in red and duplications in blue. The bottom part of the visualization depicts the depth of read coverage at each 50 kbp window. The read coverage of the data used in this visualization was 1×

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BMC Genomics

ISSN: 1471-2164

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