Blog articles

The impact of Covid-19 on rare disease communities

Guest author Dr Christine Patch explains the challenges in supporting patients with rare disease during the pandemic, as well as the opportunities that may arise

Sepsis and the genome

Recent studies on sepsis show that genomics could hold the key to faster diagnosis and treatment, as well as understanding why it occurs
Drawing a family history

10 things to consider when offering a genomic test

Guest author Professor Frances Flinter explains 10 of the most important considerations for professionals and patients

Genomics in nursing: making a difference to patients

As part of this year’s #GenomicsConversation, guest author Leanne LeRiche shares her family’s experience of genomic testing, and the vital role that nurses play
Doctor with patient

GEP fellow publishes research on patient experience

Lisa Ballard and her co-authors hope their findings about the consent process for genomic testing will inform the new NHS Genomic Medicine Service

What is whole exome sequencing?

Following the recent NHS announcement that WES will be used for critically ill babies and children, we explore what it is and the benefits it could bring

Genomics: combating coronavirus

In the second of two articles focusing on the recent coronavirus outbreak, we explore how genomics is being put to use in diagnosis and treatment

Whole genome sequencing drives progress in cancer

A new study into metastatic cancers highlights the significant potential for WGS in deepening understanding of the disease and improving treatment options

News articles

Master’s in Genomic Medicine: 2020/21 funding opens

The funding application process is now live for Master’s-level CPPD modules and qualifications in genomics at partner universities