Closed

Genetics Outsourcing of Next Generation Sequencing

The Newcastle Upon Tyne Hospitals NHS Foundation Trust · £480,000 · closes 19 Jul 2024

£480,000

Estimated value

Closed

Deadline

19 Jun 2024

Published

This tender has closed.

See what's open in architecture and engineering services, or get contracts like this in your inbox each morning — free.

Set up free alertsOpen architecture and engineering services tenders

About this contract

The Northeast and Yorkshire Genomics Laboratory Hub (NEY GLH) is a partnership between Newcastle Teaching Hospitals, Leeds Teaching Hospitals and Sheffield Children’s Hospital Trusts, providing genomic diagnostic services across the region. The combined services offer a range of both core and specialist diagnostic services. The GLH is looking to procure rare disease genomic testing in line with the national test directory to support key service delivery NHS England » National genomic test directory.<br/><br/>To analyse and report Single Nucleotide Variant and Copy Number Variant data for all required genes on relevant NHS PanelAPP at a minimum of 30x coverage for >95% of regions targeted. <br/><br/>Panels required: <br/>MSK R101 Ehlers Danlos syndrome with a likely monogenic cause<br/><br/>MSK R102 Osteogenesis imperfecta<br/><br/>Resp R188 Pulmonary Arterial Hypertension<br/><br/>Resp R189 Respiratory ciliopathies including non-CF bronchiectasis<br/><br/>Resp R421 Pulmonary Fibrosis Familial

Key dates

Published19 Jun 2024
Submission deadline19 Jul 2024 Add to calendar ↓

Source

Source notice on Find a TenderView ↗

Lot — bid on it if it fits

This contract has one lot. Bid if it suits your firm.

The Northeast and Yorkshire Genomics Laboratory Hub (NEY GLH) is a partnership between Newcastle Teaching Hospitals, Leeds Teaching Hospitals and Sheffield Children’s Hospital Trusts, providing genomic diagnostic services across the region. The combined services offer a range of both core and specialist diagnostic services. The GLH is looking to procure rare disease genomic testing in line with the national test directory to support key service delivery NHS England » National genomic test directory.<br/><br/>To analyse and report Single Nucleotide Variant and Copy Number Variant data for all required genes on relevant NHS PanelAPP at a minimum of 30x coverage for >95% of regions targeted. <br/><br/>Panels required: <br/>MSK R101 Ehlers Danlos syndrome with a likely monogenic cause<br/><br/>MSK R102 Osteogenesis imperfecta<br/><br/>Resp R188 Pulmonary Arterial Hypertension<br/><br/>Resp R189 Respiratory ciliopathies including non-CF bronchiectasis<br/><br/>Resp R421 Pulmonary Fibrosis Familial£480,000

Who to contact

NameEwan Bond
Phone+44 1912138916

Similar open tenders

Contains public sector information licensed under OGL v3.0