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Fig. 1 | Genome Biology

Fig. 1

From: TADA—a machine learning tool for functional annotation-based prioritisation of pathogenic CNVs

Fig. 1

Enrichment Analysis of non-pathogenic and pathogenic deletions. The figure shows the log2(fold change) for expected and observed variant overlap for each set of genomic annotations based on 10,000 simulations. The size of the squares on the right side of the figure is proportional to the overlap FC difference between pathogenic and non-pathogenic deletions. Grey bars and squares indicate a non-significant FC (q value ≤ 0.01)

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