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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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DataCite Commons2024-02-08 更新2024-07-28 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
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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).
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figshare
创建时间:
2020-01-16
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