HDI are working with the Institute of Genetic Medicine at Newcastle University and Public Health England to help establish a national Lynch Syndrome Registry to support patients and researchers.
HDI is pleased to be contributing to the CanGene CanVar programme, a five-year project to centralise data and create an interface between the NHS and research groups which will underpin future expansions in genetic testing.
BRCA Challenge development resource for pseudonymisation
The BRCA Challenge is a global initiative to understand all the mutations in the BRCA genes, which can predispose individuals for ...
N- and K-RAS gene mutation data collection
HDI collects data about N- and RAS gene mutations to support the National Cancer Registration and Analysis Service (NCRAS). Further details: The analysis of RAS gene...
Collecting EGFR status from molecular testing laboratories
EGFR status is an increasingly important analysis for patients diagnosed with lung cancer. The receptor status and ...
ALK gene mutation data collection
HDI collects data about ALK gene mutations to support the National Cancer Registration and Analysis Service (NCRAS). Further details: The analysis of ALK mutations in patients...
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