Welcome to MOCR-DB
Multi-Omics Causal Resource DataBase
About MOCR-DB
- The Multi-Omics Causal Resource Database (MOCR-DB) is an integrated resource for investigating genetic correlation, causal inference, and functional interpretation across complex traits. It provides a platform to explore phenotype-to-phenotype genetic relationships and phenotype-to-gene associations with functional mechanisms, leveraging large-scale genomic data.
- MOCR-DB integrates summary statistics from large-scale resources, including FinnGen, UK Biobank, and COVID-19 HGI.
- The current version includes:
- ~600 GWAS datasets across diverse traits;
- ~24,000 MR results (with ~1,200 nominally significant);
- ~33,000 LDSC trait pairs (with ~13,000 showing significant correlation);
- ~740,000 significant SMR gene-trait associations (based on xQTLs data).
- An AI-assisted module provides plain-language summaries to contextualize statistical findings.
- MOCR-DB supports network construction to visualize shared genetic architecture and functional mediators across traits.
GWAS Datasets
~600
Data Sources
3 Databases
xQTL
53
MR
Significant: 1,200
LDSC
Significant: 13,000
SMR
Significant: 740,000