This article covers a funding round on 17 September 2025 for Enhanced Genomics, a Cambridge-based company developing a 3D multi-omics platform that maps disease-associated genetic variants in three dimensions, founded by Stefan Schoenfelder and Peter Fraser. It raised £13.9m, with investors not disclosed.
A 3D multi-omics platform that maps disease-associated genetic variants in three dimensions in human cell types. It converts genetic variation outside genes into candidate drug targets for drug discovery.
Researchers and drug developers face difficulty linking non-coding genetic variants to disease mechanisms and drug targets. This gap hinders target discovery for common diseases, including autoimmune disorders.
Enhanced Genomics helps by mapping disease-linked variants in three dimensions in relevant human cell types. Its 3D multi-omics platform converts non-coding variation into precise, testable drug targets genome-wide.
Enhanced Genomics raised £13.9m ($19m).
Key investors in the round include the following:
If you're researching potential backers in this space:
The founders of Enhanced Genomics are Stefan Schoenfelder and Peter Fraser.
Enhanced Genomics Ltd is based in Cambridge, UK.
Enhanced Genomics operates in the drug discovery sector. This sector finds and develops new medicines. It looks for the parts of the body medicines can affect to treat illness.
Key trends and challenges in Genomics:
Scientists now combine DNA, RNA and protein data with 3D genome maps to link variants to genes. For example, mapping chromosome folding shows which distant variant controls a specific gene.
Multiple technologies offer different insights, creating competition and choice for researchers and developers. For example, single-cell, spatial and genome-wide studies trade off resolution and speed.
Many platform discoveries have not yet become late-stage drug candidates, slowing clinical impact. Building cell-type specific maps requires heavy data infrastructure and extensive lab validation.
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