Helix

Helix Genomics API

Partner-gated programmatic access to Helix Exome+ sequencing data - more than 100 million base pairs including SNPs, indels, and copy number variants, with panel-grade coverage of clinically important regions such as the ACMG actionable genes, carrier screening, hereditary cancer, and hereditary cardiovascular disease. Access is provisioned through Helix partnerships; no public base URL or OpenAPI specification is published, so endpoints are modeled from Helix product documentation.

GitHub

Documentation

📖
Documentation
https://genomics.helix.com/

Other Resources

🔗
Website
https://www.helix.com/health-systems
🔗
APIsJSON
https://raw.githubusercontent.com/api-evangelist/helix-genomics/refs/heads/main/apis.yml

API entry from apis.yml

apis.yml Raw ↑ 
aid: helix-genomics:helix-genomics-api
name: Helix Genomics API
tags:
- Genomics
- Variants
- Sequencing
- Exome
image: https://kinlane-images.s3.amazonaws.com/shared/apis-json/apis-json-logo.jpg
humanURL: https://genomics.helix.com/
properties:
- url: https://genomics.helix.com/
  type: Documentation
- url: https://www.helix.com/health-systems
  type: Website
description: Partner-gated programmatic access to Helix Exome+ sequencing data - more than 100 million
  base pairs including SNPs, indels, and copy number variants, with panel-grade coverage of clinically
  important regions such as the ACMG actionable genes, carrier screening, hereditary cancer, and hereditary
  cardiovascular disease. Access is provisioned through Helix partnerships; no public base URL or OpenAPI
  specification is published, so endpoints are modeled from Helix product documentation.