Skip to main content
Fig. 2 | BMC Genomics

Fig. 2

From: A validated generally applicable approach using the systematic assessment of disease modules by GWAS reveals a multi-omic module strongly associated with risk factors in multiple sclerosis

Fig. 2

Genomic concordance of MODifieR modules on transcriptomic datasets. (a) Heatmap of PASCAL p-values for eight single-method and eight consensus MODifieR modules, identified for 47 publicly available transcriptomic datasets. Module performance P-values are shown in a white to blue scale, where any shade of blue represents a significant module (< 0.05; the darker, the more significant), white represents a non-significant module, and grey represents a module of size zero. Datasets are classified into six disease types: cardiovascular (red), glycemic (golden), inflammatory (green), neurodegenerative (fuchsia), psychiatric and social (pink), autoimmune (dark purple), and others (light purple); and two cell types: blood (maroon), and others (light yellow). Datasets are ranked by meta-P-values using Fisher’s method of the single-method module P-values across and within their disease types (dataset score, bottom boxplot). MODifieR methods are organized by algorithm type: seed-based (green), co-expression-based (yellow), and clique-based (red), plus the consensus modules (blue). Single-methods and consensus were scored by meta-P-values across datasets (method score, right boxplot). Consensus x/8 indicates that the module genes are found in at least x methods out of eight. (b) Scatter plot showing Spearman correlation between module score and betweenness centrality. Modules are represented with a different shape depending on their method and colored based on the disease type. (c) Scatter plot showing Spearman correlation between module score and module size. Modules are represented with a different shape depending on their method and colored based on the disease type

Back to article page