Tool Catalog

Publicly available web tools (no FinnGen account needed):

Tool
Brief summary

Core endpoint definitions and relationships between endpoints. Results from CodeWAS and LabWAS tools and mortality from FinRegistry. Includes also Kanta lab data and their distributions.

Tool to understand the relationships between FinnGen core endpoints

Multiple Manhattan Plot to align and browse between 2 to 20 GWAS scans

Lightweight Association Viewer Across Ailments to display PheWAS results for a variant as a volcano plot

A site detailing the FinnGen data mapping to the OMOP common data model (CDM)

Look up availability and OMOP mapping of Kanta lab tests

Repository of the codes for the FinnGen analyses

Browse publicly available GWAS results (note there are PheWebs available for multiple FinnGen releases, to access the earlier release browsers visit https://www.finngen.fi/en/access_results)

Browse FinnGen-UKBB GWAS meta-analysis results

Browse FinnGen-MVP-UKBB GWAS meta-analysis results

Variant Cluster Call Corrector

Web tools for FinnGen green data accounts:

Tool
Brief summary

Download the accumulated FinnGen core analysis results from the Google console

Browse core GWAS results, conditional analysis, finemapping, colocs

Browse GWAS results for user-defined phenotypes

Additive and recessive phenotype associations for rare and common coding variants

Tool to annotate lead variants with phenotype associations, eQTLs, pQTLs and splice QTLs

Endpoint GWASs separately for females/males and test for different effect sizes

Browse core GWAS results from recessive analysis

Sandbox environment and tools for FinnGen red data accounts:

Tool
Brief summary

Trusted Research Environment (TRE), access to FinnGen individual level data

OHDSI/OMOP tool to define concept sets and cohorts

Import cohorts created elsewhere and explore and operate them, e.g. by using CodeWAS and TimeCodeWAS. Launch GWAS.

View the health history of an individual

Trajectory Visualization Tool to view the health trajectories of a cohort of individuals

View, edit and export genotype data

Command line tool to assist users running custom GWAS. The easiest way to launch CustomGWAS is through the Cohort Operations tool.

GUI to help with running Regenie, Finemapping, GATE, etc.

View polygenic scores for existing endpoints or a custom cohort

Tool for validating the format of user custom GWAS summary stats to be viewable in a PheWeb-style

A command line interface allowing users to query carriers of variants in FinnGen exome data

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