Comprehensive Library |
Comprehensive collection and deep annotation of results from
65 mGWAS publications.
Support for searching a single item, exploring individual studies, and uploading a list.
Integrating with HaploReg, VEP,
KEGG, Transporter Classification Database (TCDB),
Recon3D as well as common PPI databases.
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Network Analysis |
Mechanistic insights: users can easily create SNP-based,
gene-based, or metabolite-based networks
and visually explore the results in a systems biology context.
Hypothesis generation: users can include known diseases associated with SNPs, genes or metabolites to
perform cross-phenotype association analysis.
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Functional Insights |
Users can perform various functional analysis including
SNP set enrichment analysis, gene set enrichment analysis,
and metabolite set enrichment analysis.
Other features including topology analysis, searching different paths
connecting SNPs, genes, metabolites, and diseases.
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News & Updates |
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Fixed bugs and updated SNP-gene-metabolite network in the SNP module (07/15/2022);
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Code cleaning and refactoring for better performance (05/31/2022);
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Added support for metabolite-disease and gene-disease network (05/23/2022);
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Updated tutorials and FAQs (05/13/2022);
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Fixed issues with table browsing and table statistics (05/10/2022);
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Fixed issues with highlighting seed nodes function (05/10/2022);
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