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Fig. 4 | BMC Genomics

Fig. 4

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

Fig. 4

Visualization of the CNVs detected in the cell line data with the six algorithms along with the array-based benchmark CNVsin the respective chromosomal locations. a Karyotypically abnormal (H9-AB) and b normal (H9-NO) variants of the human embryonic stem cell line H9 were analysed. Deletions are marked in red and gains in blue. The bottom part of the visualization depicts the depth of read coverage at each 50 kbp window

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BMC Genomics

ISSN: 1471-2164

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