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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
Supplementary Material for: Model-Based Multifactor Dimensionality Reduction for Rare Variant Association Analysis
Genome-wide association studies have revealed a vast amount of common loci associated to human complex diseases. Still, a large proportion of heritability remains unexplained. The extent to which rare
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DNA methylation in colon mucosa samples from individuals with Crohns' disease or ulcerative colitis and normal controls
DNA methylation in colon mucosa samples from individuals with Crohns' disease or ulcerative colitis and normal controls
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Subgroup analysis of the association between the STAT3 rs744166 polymorphisms and the risk of UC.
HB, hospital-based; PB, population-based; Bonferroni, P-value in Bonferroni testing; FDR, P-value in false discovery rate. Subgroup analysis of the association between the STAT3 rs744166 polymorphisms
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Genotype and allele frequencies of rs4552569 and rs17095830 in AS patients with or without inflammatory bowel disease (IBD).
*Significant (P<0.025) values are in bold.
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Supplementary Material for: Population Genetics of Rare Variants and Complex Diseases
Objectives: Identifying drivers of complex traits from the noisy signals of genetic variation obtained from high-throughput genome sequencing technologies is a central challenge faced by human genetic
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