Additional file 2 of Oxidative stress gene expression, DNA methylation, and gut microbiota interaction trigger Crohn’s disease: a multi-omics Mendelian randomization study
posted on 2023-05-12, 03:39authored byShu Xu, Xiaozhi Li, Shenghong Zhang, Cancan Qi, Zhenhua Zhang, Ruiqi Ma, Liyuan Xiang, Lianmin Chen, Yijun Zhu, Ce Tang, Arno R. Bourgonje, Miaoxin Li, Yao He, Zhirong Zeng, Shixian Hu, Rui Feng, Minhu Chen
Additional file 2: Table S1. Characteristics of six transcriptome datasets used in the study. Table S2. 817 OS-related genes with a relevance score ≥ 7 obtained from GeneCards. Table S3. Meta-analysis of 708 differentially expressed OS genes from six datasets. Table S4. Cell type-specific expression analysis (CSEA) of 438 intestinal OS DEGs. Table S5. Summary-based Mendelian randomization (SMR) analysis from blood gene expression to CD (FDR < 0.05). Table S6. SMR analysis from blood DNA methylation to CD (FDR < 0.05). Table S7. SMR analysis from blood DNA methylation to gene expression (FDR < 0.05). Table S8. Regulatory component annotation of 665 DNA methylation sites. Table S9. Meta-analysis between GTEx and 1000IBD intestinal cis-eQTLs (FDR < 0.05). Table S10. SMR analysis from intestinal gene expression to CD (FDR < 0.05). Table S11. Colocalization analysis between gene expression and gut microbiota (PPH4 > 0.5). Table S12. Demographic characteristics of FAH-SYS IBD multi-omics cohort. Table S13. External cohort validation: intestinal DEG results between CD and HC. Table S14. External cohort validation: associations between intestinal gene expression and gut microbiota.
Funding
National Natural Science Foundation of China Natural Science Foundation of Guangdong Province Leona M. and Harry B. Helmsley Charitable Trust