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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

Fig. 1

Workflow of CNV analysis and candidate genes discovery. CNV calls by DNA Analytics were performed by using the ADM2 algorithm, with a sensitivity threshold of 6.0 and a minimum of 5 probes. The QC metrics table was used to check signal intensity and background noise. Above 0.22 of DLR Score (Derivative Log Ratio) was set as the cutoff to avoid false CNVs. 6 cases were removed because of bad quality of data during the QC filter.6 cases with aneuploid abnormals (Trisomy X and Down syndrome) were not put into further analysis

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BMC Medical Genomics

ISSN: 1755-8794

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