A massive effort using exome sequencing data from more than 450,000 UK Biobank participants has revealed rare and common gene […]
In the latest episode of Genetics Unzipped, presenter Dr Kat Arney takes a look at how we learned to read […]
Stephen F. Kingsmore is the President and CEO of Rady Children’s Institute for Genomic Medicine, where they are pioneering the […]
How the human embryo develops is a complex and unclear phenomenon. Scientists are faced with many challenges when it comes […]
A new study, published today in JAMA Pediatrics, has investigated the impact of newborn genomic sequencing (nGS) on parents. Their […]
A new study, published in Nature Medicine, has found that driver mutations in metastatic cancer genomes remain stable over time. […]
Illumina’s systems employ short-read sequencing techniques, which has been the predominant NGS technology for the last decade. The company has […]
Introduction It has been over 30 years since the first generation of DNA sequencing technology was developed in 1977. Since […]
Heidi Rehm is the Chief Genomics Officer in the Department of Medicine and at the Center for Genomic Medicine at […]
Dame Janet Thornton is a Senior Scientist and Emeritus Director of EMBL-EBI. Thornton is a pioneer in structural bioinformatics, having […]
