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Patient Perspectives: Vaila Morrison – Architect, Mother and Rare Disease Advocate (KAT6A syndrome)

Vaila Morrison is an architect focused on sustainable and inclusive design as well as a mother to a child with […]

World of Genomics: The United Kingdom

Being a UK based company in the genomics field, we know the space here better than in any other country […]

Sample Preparation for NGS – A Comprehensive Guide

Introduction Sample preparation is the process of getting DNA ready for Next Generation Sequencing (NGS). This requires a few steps… […]

Non-syndromic cleft lip aetiology is illuminated by integrative approaches

In a recent study, researchers integrated existing genomic, epigenomic and transcriptomic data to generate novel insights into the aetiology of […]

Genomics week in brief: Week ending 24th April

We have gathered all the best and latest genomics news and research from the past week, and put it here, […]

The Rarest of the Rare

In Europe, a rare disease is defined rare when it affects fewer than 1 in 2,000 people. However, this definition […]

Be more positive: give blood

Last weekend vampires and witches came out to play. People smeared litres of fake blood on their faces and doors. […]

DNA Today Podcast: DTC Series wrap up

DNA Today has just wrapped up their second series of 2020, exploring the landscape of direct-to-consumer (DTC) genetic testing over […]

Genome UK: The future of healthcare

Genome UK The UK has launched its new National Genomic Healthcare Strategy, with the goal of cementing its status as […]