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资源简介：
Overview of known rare IBD risk variants.
应用场景：
创建时间：
2016-08-04
相关数据集
Genotype frequencies of CNR1 1359 G/A (p.Thr453Thr) polymorphism in patients with Crohn's disease (CD) and ulcerative colitis (UC) as well as in controls.
Genotype frequencies of CNR1 1359 G/A (p.Thr453Thr) polymorphism in patients with Crohn's disease (CD) and ulcerative colitis (UC) as well as in controls.
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DataSheet_2_Experimental and genetic evidence for the impact of CD5 and CD6 expression and variation in inflammatory bowel disease.csv
Crohn’s disease (CD) and ulcerative colitis (UC) are inflammatory bowel diseases (IBD) resulting from the interaction of multiple environmental, genetic and immunological factors. CD5 and CD6 are para
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Gene Set Enrichment Analysis (GSEA) of protein VES calculated on ClinVar/COSMIC/common/rare variant sets.
(Data underlying Figs 4 and 6A–6D and S5). (XLSX)
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Additional file 8 of Smarcad1 mediates microbiota-induced inflammation in mouse and coordinates gene expression in the intestinal epithelium
Additional file 8: Table S7. Differential H3K9me3 MACS-peaks identified with the EdgeR test (cut-off FDR < 0.00001) on comparison of ChIP-seq datasets from WT and Smarcad1-KO (Villin-cre mediated) col
Figshare2020-03-11 更新30
Whole genome sequencing of Crohn s disease patients
Population based sequencing of whole genomes of Crohn's disease patients.EGA study EGAS00001000065
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