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MOESM7 of De novo variants in exomes of congenital heart disease patients identify risk genes and pathways

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Mendeley Data2024-06-27 更新2024-06-27 收录
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https://springernature.figshare.com/articles/dataset/MOESM7_of_De_novo_variants_in_exomes_of_congenital_heart_disease_patients_identify_risk_genes_and_pathways/11626521/1
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Additional file 7: Enrichment analysis in CTD and LVO: Table S29. IPA canonical pathways among 59 genes in conotruncal defects (CTD), Table S30. InnateDB pathway analysis among 59 genes in conotruncal defects (CTD), Table S31. InnateDB GO analysis among 59 genes in conotruncal defects (CTD), Table S32. NetworkAnalyst PPI Network among 59 genes in conotruncal defects (CTD), Table S33. Priority scores of 59 genes in conotruncal defects (CTD), Table S34. IPA canonical pathways among 68 genes in left ventricular outflow tract obstruction (LVO), Table S35. InnateDB pathway analysis among 68 genes in left ventricular outflow tract obstruction (LVO), Table S36. InnateDB GO analysis among 68 genes in left ventricular outflow tract obstruction (LVO), Table S37. NetworkAnalyst PPI Network among 68 genes in left ventricular outflow tract obstruction (LVO), Table S38. Priority scores of 68 genes in left ventricular outflow tract obstruction (LVO).

附加文件7:圆锥动脉干缺损(conotruncal defects,CTD)与左心室流出道梗阻(left ventricular outflow tract obstruction,LVO)的富集分析: 表S29:圆锥动脉干缺损(CTD)相关59个基因的IPA经典通路分析; 表S30:圆锥动脉干缺损(CTD)相关59个基因的InnateDB通路分析; 表S31:圆锥动脉干缺损(CTD)相关59个基因的InnateDB基因本体(Gene Ontology,GO)分析; 表S32:圆锥动脉干缺损(CTD)相关59个基因的NetworkAnalyst蛋白质相互作用(Protein-Protein Interaction,PPI)网络分析; 表S33:圆锥动脉干缺损(CTD)相关59个基因的优先级评分; 表S34:左心室流出道梗阻(LVO)相关68个基因的IPA经典通路分析; 表S35:左心室流出道梗阻(LVO)相关68个基因的InnateDB通路分析; 表S36:左心室流出道梗阻(LVO)相关68个基因的InnateDB GO分析; 表S37:左心室流出道梗阻(LVO)相关68个基因的NetworkAnalyst PPI网络分析; 表S38:左心室流出道梗阻(LVO)相关68个基因的优先级评分。
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2023-06-28
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