Coexpression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 7.
Figure 7.

Coexpression network organization of ASD genes with dnLoF mutations in NPCs, and epilepsy genes with dnMis mutations in interneurons. (A) Spearman's correlation with dnLoF-ASD genes in NPCs for ASD genes with ≥3, 2, 1, and 0 dnLoF mutations. (B) Spearman's correlation with dnMis-Epi genes in interneurons for epilepsy genes with ≥2, 1, and 0 dnMis mutations. (C) Coexpression network of ASD genes with at least one dnLoF mutation in NPCs. Red, green, and blue nodes indicate ASD genes with ≥3, 2, and 1 dnLoF mutations, respectively. Red, green, and blue edges indicate coexpression within ASD genes with ≥3, 2, and 1 dnLoF mutations, respectively, and orange edges indicate coexpression between ASD genes with ≥3 dnLoF mutations and ASD genes with 2 dnLoF mutations. (D) Coexpression network of epilepsy genes with at least one dnMis mutation in interneurons. Red and blue nodes indicate epilepsy genes with ≥2 and 1 dnMis mutations, respectively. Red and blue edges indicate coexpression within epilepsy genes with ≥2 and 1 dnMis mutations, respectively. In C and D, node size is proportional to coexpression degree. (E) Coexpression degree in the NPC network of ASD genes with ≥3, 2, and 1 dnLoF mutations. (F) Coexpression degree in the interneuron network of epilepsy genes with ≥2 and 1 dnMis mutations. In A,B,E,F, P-values were calculated using the one-sided Wilcoxon rank-sum test.

This Article

  1. Genome Res. 30: 835-848

Preprint Server