MOESM6 of De novo variants in exomes of congenital heart disease patients identify risk genes and pathways
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https://springernature.figshare.com/articles/dataset/MOESM6_of_De_novo_variants_in_exomes_of_congenital_heart_disease_patients_identify_risk_genes_and_pathways/11626512/1
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Additional file 6: Enrichment analysis in isolated and syndromic CHD: Table S19. IPA canonical pathways among 64 genes in isolated CHD cases, Table S20. InnateDB pathway analysis among 64 genes in isolated CHD cases, Table S21. InnateDB GO analysis among 64 genes in isolated CHD cases, Table S22. NetworkAnalyst PPI Network among 64 genes in isolated CHD cases, Table S23. Priority scores of 64 genes in isolated CHD cases, Table S24. IPA canonical pathways among 105 genes in syndromic CHD cases, Table S25. InnateDB pathway analysis among 105 genes in syndromic CHD cases, Table S26. InnateDB GO analysis among 105 genes in syndromic CHD cases, Table S27. NetworkAnalyst PPI Network among 105 genes in syndromic CHD cases, Table S28. Priority scores of 105 genes in syndromic CHD cases.
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figshare
创建时间：
2020-01-16
