MOESM5 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/MOESM5_of_De_novo_variants_in_exomes_of_congenital_heart_disease_patients_identify_risk_genes_and_pathways/11626506/1
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资源简介：
Additional file 5: Gene prioritization: Table S16. Priority scores of 127 genes in cases, Table S17. Priority scores of 127 genes in CHD cases based on human CHD genes only, Table S18. Average biological distance of each candidate gene to human and mouse CHD genes based on Human Gene Connectome.
提供机构：
Itan, Yuval; Tristani-Firouzi, Martin; Gelb, Bruce; Sevim Bayrak, Cigdem; Zhang, Peng
创建时间：
2020-01-16
