Curated literature based database of germline human genomic variants database
Buyer: NHS England
- Published
- 5 October 2026
- Estimated value
- £2,347,766
- Lots
- 1
- Notice number
- 093928-2026
- Reference
- ocds-h6vhtk-0780fb
- Official source
- Official source
CPV codes
- 72320000Database services
Description
The requirement is for a database or a tool that clinicians can use to search for rare inherited disease mutations, or search for an overview of known mutations associated with a particular disease, interpreting clinical test results, looking for the likely causal mutation in a list of variants, or seeking to integrate mutation content into your custom NGS pipeline or data repository. The Database or tool will need to work by collating all published variants into a detailed repository of information. It should easily allow for variants to be listed using transcripts, to ensure that scientists can easily search for the variant they are researching which enormously reduces scientific analytical time, and in turn turn around times for patients.
Official publications
- FTS · 093928-2026 · 5 October 2026
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Frequently asked questions
- What is the estimated value of this tender?
- The estimated value published by the buyer is £2,347,766.
- Who is the buyer of this tender?
- The contracting authority is NHS England (United Kingdom).
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- Bids are submitted through the official public procurement portal in the United Kingdom. El Vínculo helps you find tenders and analyse their documents; submission always happens at the official source.
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