Comprehensive Libraries |
Comprehensive collection and deep annotation of results from
65 mGWAS publications.
Integrated with HaploReg, VEP,
KEGG, Transporter Classification Database (TCDB),
Recon3D as well as common PPI databases.
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Functional Insights |
Create and visually explore SNP-based,
gene-based, or metabolite-based networks.
Perform SNP set enrichment analysis, gene set enrichment analysis, or metabolite set enrichment analysis.
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Causal Inference |
Leverage known diseases associated with SNPs, genes or metabolites to
perform cross-phenotype association analysis
or causal inference based on two sample Mendelian randomization.
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