Our Mission

Unravel links between genetic variations and idiopathic symptoms

In 2025, a small team of biologists and engineers formed Genoxus Lab, a nonprofit corporation, to help people with genetic variation-based diseases by understanding their genetic makeup. By delving into public databases and research articles, we created a detailed map of relationship between genetic variations and diseases or human traits.

Current commercial human genetic testing workflows, starting from either Whole Genome Sequencing (WGS) or Whole Exome Sequencing (WES) data, provide disease-specific analyses by restricting genetic assessment to preset gene panels, which only include genes whose variations are well-known to be disease-related. These tests can be useful in diagnosing targeted diseases but often leave other complications unaddressed. As a result, it is difficult for medical care providers to obtain a full picture of their patients’ conditions.

We built a platform that processes WGS and WES data, identifies genetic variants, and constructs a comprehensive map of genetic variant to disease and trait associations. We make this platform accessible to patients and their healthcare providers to promote understanding of genetically based symptoms and highlight disease-prone risk variants.

We take patient privacy seriously. Our platform is designed to safeguard patient data as we actively prepare for HIPAA compliance certification.

We welcome your help and contribution to further develop our platform, and bring more values to patients and healthcare providers. Please consider contributing to this efforts with donations or collaborations.