Cloud service for interpretation of genetic variants for Helse Bergen HF
Buyer: SYKEHUSINNKJØP HF
- Published
- 12 January 2024
- Submission deadline
- 29 January 2024
- Place of performance
- NO0A2
- Procedure
- open
- Lots
- 1
- Notice number
- 00023928-2024
- Reference
- 35e9ee4a-4bf2-49a6-b2e2-f12df2ffca55
- Official source
- Official source
CPV codes
- 72000000Servicios TI: consultoría, desarrollo de software, Internet y apoyo
- 48180000Paquetes de software médico
- 72400000Servicios de Internet
- 72410000Servicios de proveedor
- 72416000Proveedores de servicio de aplicaciones
Description
The Customer's Department of Medical Genetics (MGM) and the Department for Cancer Genomics (SQG) provide NGS-based diagnostic services for medical conditions arising from somatic and germline variants. Our NGS-based diagnostic approach involves both whole exome sequencing (WES) and targeted panels. In addition, we are performing copy number analysis (CNV), based on SNP array data generated using the Affymetrix platform. Our current analysis tools, Alissa and Bench software, are used for variant interpretation. We are now seeking an alternative system that can replace, and potentially surpass or enhance the functionalities of these tools. Our needs include:Filtration, annotation, and classification of germline variants generated by NGS. Filtration, annotation, and classification of somatic variants generated by NGS. Filtration, annotation, and classification of germline and somatic CNVs generated by SNP-Arrays.University Hospital of North Norway (UNN) has option to purchase.
Frequently asked questions
- What is the deadline to bid for this tender?
- The submission deadline is 29 January 2024. Check the official source, as dates can be modified.
- Who is the buyer of this tender?
- The contracting authority is SYKEHUSINNKJØP HF (European Union).
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