What’s been going on in the life sciences world this week? Check out Week in Brief for an overview of the biggest news from ...

The BabySeq project was a first-of-its-kind initiative that used a randomised clinical trial format to assess the utility of genomic sequencing to identify disease risk in newborns. At The Festival of ...

Written by Arpita Kulkarni (Director of the Functional Genomics and Bioinformatics Core at HMS/BIDMC). Across the life sciences, a quiet anxiety is growing: what is the role of the experimental ...

Next generation sequencing has become a fundamental approach in many aspects of life science research and impressive innovation continues to push the boundaries even further. We are pleased to ...

Join us for Unlocking Precision Oncology’s through Next-Gen Molecular Analysis, which showcases cutting-edge advances in diagnostics, molecular profiling and therapy resistance, revealing how adaptive ...

This feature was written using content from out recenty published Proteomics Playbook, which you can download for FREE here. The sequence of a protein is critical as it largely dictates the protein’s ...

Analysis of proteins is not simple. Unlike DNA, there is incredible diversity in the concentration and variety of proteins created by a cell at any given moment. In our Proteomics Playbook we outline ...

At our recent FOG Live: Single Cell and Spatial event, Aridiman Pandit (Senior Principal Research Scientists, AbbVie) explored how single-cell and multi-omics technologies can revolutionise drug ...

The Festival of Genomics and Biodata is just around the corner, and we’ve had the opportunity to sit down with some of our expert speakers to get a sneak peek into what they’ll be discussing, and why ...

Bigger and better than ever before, The Festival of Genomics & Biodata is returning to London in January 2025! It’s hard to believe that the first Festival was 10 years ago, and it’s come a remarkably ...

Next generation sequencing (NGS) is a powerful tool for uncovering a patient’s inherited susceptibility to cancer, paving the way for more effective prevention strategies. However, hereditary cancer ...

Pinpointing pathogenic mutations from large, complex datasets can be difficult, time consuming and somewhat overwhelming. So, how can you best streamline your genomic analysis, to make it quicker, ...