Curated literature based database of germline human genomic variants database
- Buyer
- NHS England
- Country
- United Kingdom
- Value
- 2.3m GBP
- Published
- 2026-10-05
- Type
- UK2 Preliminary market engagement notice
- Status
- Open to bid
- Category
- CPV 72320000
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.
The buyer's description as published on Find a Tender (UK). The full notice is at the source.
Around this tender
- NHS England has 64 notices on this site, 19 of them open now, the earliest published 2026-10-05. See them all.
- One of 209 open IT, software & data tenders in United Kingdom on this site; where a value is published, the median is 833.3k USD.
- Work under the same CPV group (723) is open in 21 other countries: Poland (18), Italy (15), Spain (12), France (10), Czechia (8) and 16 more.
Counted from the notices this site holds, which reach back about a month - not everything a buyer has ever published.
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About this record
This notice was published via Find a Tender (UK) and indexed automatically. Figures and dates are reproduced as published at source; always confirm against the original before acting on a deadline.