In Europe, a rare disease is defined rare when it affects fewer than 1 in 2,000 people. However, this definition […]
The ease of new gene editing technologies has opened opportunities to explore in more detail the genetic underpinnings of disease, […]
Another round-up of the latest genomics news and research from the past week – enjoy! Top stories from the past […]
Using whole-exome sequencing (WES), researchers have identified underlying variants in children with rare genetic paediatric diseases. Rare genetic paediatric diseases […]
Written by Anja Brunner (Marketing Manager at Samplix) Genome editing Undoubtedly, advances in gene editing have allowed us to imagine a […]
The genomic sequencing of Mammoth teeth preserved in Eastern Siberian permafrost have produced the oldest ancient DNA on record. Genomic […]
The Human Genome Project Published 20 years ago, the first drafts of the human genome opened the doors to a […]
A recent study, published in Nature used Genome Wide Association Studies to identify new risk loci associated with Lewy Body […]
Researchers from ChristianaCare’s Gene Editing Institute have developed a new tool – DECODR – which reveals unwanted mutations at sites […]
The latest ‘Genomics week in brief’ filled with the most recent genomics news and research from the past week! Top […]
