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Developing effective ctDNA testing services for lung cancerReportOur report outlines the most pressing issues affecting the implementation and provision of ctDNA testing services for lung cancer and describes the early experiences of some of the laboratories
Linking and sharing routine health data for researchReportThe recommendations are drawn from a series of interviews with experienced data users on the complex issues of using de-identified data, the barriers and the ways to improve data sharing for research.
Polygenic scores, risk and cardiovascular diseaseReportPublished in 2019, this reports examines the evidence and readiness for clinical implementation of polygenic scores from the perspective of cardiovascular disease prevention.
Variant classification and interpretationReportWhether and how the American College of Medical Genetics and Genomics (ACMG) sequence variant guidelines should be adopted and implemented.
Delivering improved access to genetic testing in epithelial ovarian cancerReportThis report describes the implementing a clinical genetics-coordinated service in our region to allow improved access to BRCA1/BRCA2 testing for epithelial ovarian cancer patients
Whole genome sequencing for breast cancer risk testingReportExamining the impact of routine breast cancer risk testing using whole genome sequencing
Data sharing to support UK clinical genetics and genomics servicesReportOur recommendations for responsible and proportionate sharing of data for patient benefit
Pathogen genomics into practiceReportPioneering work on converting genomics into population wide, high quality, evidence based pathogen services. Full report, summary and policy briefings