MOESM4 of De novo variants in exomes of congenital heart disease patients identify risk genes and pathways

Additional file 4: Enrichment analyses in validation set: Table S10. De novo mutations in the filtered validation dataset, Table S11. IPA canonical pathways among 30 genes in validation dataset, Table S12. InnateDB pathway analysis among 30 genes in validation dataset, Table S13. InnateDB GO analysis among 30 genes in validation dataset, Table S14a. IPA Networks among 30 genes in validation dataset, Table S14b. NetworkAnalyst PPI Network among 30 genes in validation dataset, Table S15. InnateDB GO analysis among 30 random genes from unfiltered validation dataset.