Work package C
Design of hpv infection detection test (genomics and proteomics)
Objectives
- To develop a high-risk HPV full genotyping test.
- To validate the high-risk HPV full genotyping test for clinical cross-reactivity, specificity, sensitivity and variability.
- To develop a non-immunostaining quantitative dual protein assay.
- To validate the proteomic quantitative assay for the corresponding clinical outcome as well as cross-reactivity, specificity, sensitivity and variability.
Tasks
- Design the high-risk HPV full genotyping test
- Optimise the HPV detection assay
- Validate the HPV detection assay in the laboratory
- Design the proteomic quantitative assay
- Optimise the proteomic quantitative assay
- Determine the reference range of the proteomic quantitative assay and the clinical interpretation of its results
- Validate the proteomic quantitative assay in the laboratory
More information about this work package?
Elizaveta Padalko and Piet Cools
elizaveta.padalko@ugent.be
