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WES uncovers mutations for rare paediatric diseases

Using whole-exome sequencing (WES), researchers have identified underlying variants in children with rare genetic paediatric diseases. Rare genetic paediatric diseases […]

Week in Brief: Week Ending 5th July

Happy Monday everyone, and welcome back to Week in Brief, your stop for all the latest genomics news! Blood disorders […]

The State Of: Multi-Omics

This feature was written by Taylor Fulton-Ward. The advent of multi-omics, or the combination of different omics for analysis, has […]

World of Genomics: Canada

Article first published by Shannon Gunn, August 2021. Updated by Lyndsey Fletcher, May 2024. With thanks to Rob Annan and […]

The Single-Cell & Spatial Buyer’s Guide

Single-cell and spatial omics can be confusing! The technology is developing at an exhilarating rate, new companies are producing solutions […]

Single-cell foundation models: The next big thing?

Single-cell sequencing has already become a staple methodology for medical research. Much of this advancement has happened within, and is […]

AI in Drug Discovery 2024: Where are we now?

Back in 2020, we covered an industry analysis of the role of Artificial Intelligence in Drug Discovery. The report covered […]

Which NGS DNA Library Prep Kit should you choose?

This feature was put together using content from Chapter 2 of the 2024 Sequencing Buyer’s Guide. For an in depth […]

Diversity in Genomics: Assessing the Mosaic of Human Life

Despite our DNA only differing at around 0.1% of base pairs, human life is complex, unique and varied. Although this […]

The Sequencing Buyer’s Guide: 6th Edition

Next generation sequencing, both short reads and long reads, is undergoing a second wave of exciting developments. New short-read platforms […]