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GWAS Catalog: Beyond SNPs

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This Python monorepo contains packages and documentation designed to help users prepare non-SNP GWAS summary statistics for submission to the GWAS Catalog.

What kind of data are supported?

Type of genetic variant Supported
Single nucleotide polymorphism (SNP) ❌, see gwas-sumstats-tools
Copy number variant (CNV) ✅
Gene ✅

Using the validation CLI for bulk data processing

First, install uv, then run:

$ uvx --from gwascatalog-sumstatapp gwascatalog beyondsnp validate --help

You should see:

Validate GWAS summary statistics files for submission to the GWAS Catalog.

positional arguments:
  INPUT                 Files to validate

options:
  -h, --help            show this help message and exit
  --type {CNV,GENE}     Type of genetic variation (CNV or GENE)
  --assembly {GRCh38,GRCh37,NCBI36,NCBI35,NCBI34}
                        Genome assembly (e.g. GRCh38)
  --effect-size {beta,odds_ratio,hazard_ratio,z_score}
                        Primary effect size measure
  --allow-zero-pvalues  Accept zero as a valid p-value
  -o, --output-dir OUTPUT_DIR
                        Output directory for results (default: ./validated/)

The package is also available from PyPI. You should always install the pydantic extra:

$ pipx install "gwascatalog.sumstatapp[pydantic]"

Documentation

See our docs here. Please create an issue or email gwas-info@ebi.ac.uk if you have any questions or comments. We appreciate community feedback.

Developer notes

This repository is a uv workspace containing two Python packages:

User facing website

Building the beyond SNPs static site

Development build (assumes deployed to / on localhost:8000):

$ cd docs
$ npm run build:dev
$ npm run serve 

Production build (assumes deployed to a base URL: gwas/apps/beyond-snps)

$ cd docs
$ npm run build

Deploying the static site is pretty simple: just put the compiled assets somewhere (a bucket, a docker image, etc.).

Metadata

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