- Country: Finland
- Summary: B. Somatic Analysis
- FIT Ref No: 115234786
- Deadline: 10 Mar 2025
- Financier: Self Financed
- Purchaser Ownership: Government
- Tender Value: Refer Document
- Notice Type: Tender
- Document Ref. No.: 119803-2025
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- Description:
- The software must be able to support analysis of SNVs, indels, copy number variations (CNVs), structural variations (SVs) and regions of loss of heterozygosity (LOH). Specifically for somatic analysis, requirements also include reporting of gene fusions, microsatellite instability (MSI), homologous recombination deficiency (HRD), and tumor mutation burden (TMB). Tests are based on analysis of nucleic acids (DNA and/or RNA) extracted from patient tissue or blood samples using next generation sequencing (NGS) on either Ion Torrent or Illumina sequencers as well as array CGH based data (ISCA v2 array, Agilent Technologies), where applicable.
Doc Title: B. Somatic analysis
Contract Type: supplies - Documents:
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CLICK HERE TO LOGINB. Somatic Analysis - Finland Tender
The HUS GROUP, a Government sector organization in Finland, has announced a new tender for B. Somatic Analysis. This tender is published on FinlandTenders under FIT Ref No: 115234786 and is categorized as a Tender. Interested and eligible suppliers are invited to participate by reviewing the tender documents and submitting their bids before the deadline on 2025-03-10.
The estimated tender value is Refer Document, and full details, including technical specifications and submission requirements, are provided in the official tender documents. Ensure all submissions meet the criteria outlined to be considered for evaluation.
