Webinar for Nurses and Midwives: Lung Cancer and Genomics
This webinar is part of the Genomics Lunch and Learn series for nurses and midwives, to provide an insight into […]
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National Pathology Workshop: From diagnosis of cancer to diagnosis of Lynch syndrome
Lynch syndrome (LS) is an inherited condition caused by pathogenic variants in DNA genes which result in an increased risk […]
Solid tumour diagnosis through large gene panel testing
On 14 July 2022 the North Thames Genomic Medicine Service (GMS) held an event showcasing how genomic medicine is transforming […]
Whole genome sequencing in paediatric haematological malignancies – lessons from our first 100 cases
On 14 July 2022 the North Thames Genomic Medicine Service (GMS) held an event showcasing how genomic medicine is transforming […]
BRCA-DIRECT: Digital pathways to expand capacity for genetic testing
On 14 July 2022 the North Thames Genomic Medicine Service (GMS) held an event showcasing how genomic medicine is transforming […]
Finding the missing 95%: The national Lynch Syndrome project
On 14 July 2022 the North Thames Genomic Medicine Service (GMS) held an event showcasing how genomic medicine is transforming […]
Genomics Lunch and Learn: Lynch Syndrome
This webinar is part of the Genomics Lunch and Learn series for nurses and midwives, to provide an insight into […]
What has genomic testing ever done for us? Patient Case Studies
In this presentation aimed at Cancer MDTs, Dr Debashis Sarker presents a patient case study of Metastatic Acinar Cell Carcinoma Pancreas. […]
From bench to bedside – how can we maximise the value of genomic reports?
In this presentation aimed at Cancer MDTs, Dr Nirupa Murugaesu provides an overview of the genomic report structure and explains how […]
How can we optimise tissue samples for genomic testing and minimise failures?
In this presentation aimed at Cancer MDTs, Professor Louise Jones provides an overview of recommended sample preparation for DNA and RNA […]