# 25.09 Platform release now live!

**URL:** https://community.opentargets.org/t/25-09-platform-release-now-live/1929
**Category:** Releases
**Created:** [17 September 2025 10:59 UTC](https://community.opentargets.org/t/25-09-platform-release-now-live/1929 "2025-09-17T10:59:15Z")
**Posts on this page:** 1
**Page:** 1

<div class="post-metadata">

### Author: ![hcornu](https://dub1.discourse-cdn.com/flex017/user_avatar/community.opentargets.org/hcornu/32/716_2.png) [@hcornu](https://community.opentargets.org/u/hcornu)
#### Post date: [17 September 2025 10:59 UTC](https://community.opentargets.org/t/25-09-platform-release-now-live/1929/1 "2025-09-17T10:59:16Z")

</div>

We have just released the latest update to the Open Targets Platform — 25.09.

  

## Key stats

| Metric | Count |
| --- | --- |
| Targets | 78,726 |
| Diseases | 39,530 |
| Drugs | 18,119 |
| Evidence | 30,396,274 |
| Associations | 10,989,518 |

### Number of credible sets

| Study Type | Count |
| --- | --- |
| GWAS | 817,738 |
| sQTL | 223,500 |
| pQTL | 33,731 |
| tuQTL | 384,852 |
| eQTL | 1,349,478 |
| sceQTL | 52,744 |

  

Number of unique studies with at least one credible set: 40,288

Number of unique biosampleIDs (number of tissues/cell-types) from molQTLs: 98

## Evidence metrics for this release:

- 3,418,392 genetic evidence from [European Variation Archive (EVA)](http://www.ebi.ac.uk/eva/)

- 1,753,850 GWAS credible sets from [GWAS Catalog](https://www.ebi.ac.uk/gwas/), [FinnGen](https://www.finngen.fi/en) through Gentropy

- 3,307 genetic evidence from [Gene2Phenotype](https://www.ebi.ac.uk/gene2phenotype)

- 34,079 genetic evidence from the [Genomics England PanelApp](https://bioinfo.extge.co.uk/crowdsourcing/PanelApp/)

- 3,047 genetic evidence from [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/)

- 6,243 genetic evidence from [Orphanet](https://www.orpha.net/)

- 38,181 genetic evidence from Gene burden

- 21,685 genetic evidence from [CRISPRBrain](https://crisprbrain.org/)

- 6,744 genetic evidence from [UniProt Literature](https://www.uniprot.org/)

- 9,117 somatic evidence from [European Variation Archive (EVA)](http://www.ebi.ac.uk/eva/)

- 4,223 somatic evidence from [intOGen](https://www.intogen.org/)

- 91,572 somatic evidence from the [Cancer Gene Census](http://cancer.sanger.ac.uk/census/)

- 33,047 somatic evidence from [Uniprot](http://www.uniprot.org/)

- 573,103 drug evidence from [ChEMBL](https://www.ebi.ac.uk/chembl/)

- 237,329 expression evidence from [Expression Atlas](https://www.ebi.ac.uk/gxa/home)

- 10,188 affected pathway evidence from [Reactome](https://reactome.org/)

- 72,459 affected pathway evidence from [SLAPenrich](https://saezlab.github.io/SLAPenrich/)

- 378 affected pathway evidence from [PROGENy](https://saezlab.github.io/progeny/)

- 390 systems biology evidence from [SysBio](https://saezlab.github.io/progeny/)

- 1,300 somatic evidence from the [Cancer Genome Interpreter](https://www.cancergenomeinterpreter.org/home)

- 517 CRISPR-Cas9 (Cancer Cell Lines) evidence from Pacini et al. (2024)

- 1,196,054 mouse model evidence from [IMPC](https://www.mousephenotype.org/)

22,881,069 scientific literature evidence from co-occurrence mining in [Europe PMC](https://europepmc.org/)

For more details and numbers, [read the 25.09 blog post.](https://blog.opentargets.org/open-targets-platform-25-09-release/)