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What is Non-Genetic Inheritance?

Epigenetic mechanisms are highly complex, diverse and often poorly understood. A recent study, published in Cell, discusses the diverse features […]

Language and nomenclature: How our words shape patient experiences

Language can often be overlooked in conversations, seen only as a vessel to communicate ideas. But for many living with […]

Unlocking the Epigenome: Precision Tools for Complex Diseases

Mark your calendar for Thursday, 5th, 12th, and 19th June 2025. Epigenetic regulation is profoundly complex – varying across cell […]

Epigenetics in Healthcare & Disease

NGS is over 20 years old, yet it is harder than ever to navigate the market. With new players and new chemistries, researchers now have a powerful arsenal of tools available to them, but understanding these tools is a challenge, let alone the challenge of picking between them.
Our latest webinar series – Sequencing: A State of Play – addresses this challenge head on. If you have questions about sequencing or are looking for tips, tricks and lessons learned for the latest sequencing methods, you won’t want to miss this one.

In these early stages of progress, clear and informative dialogue between experts in the field is vital. No one has the time to read all the papers and preprints necessary to truly ‘stay ahead’. Therefore, a tailored webinar series such as this is the perfect opportunity to learn on the go. 

So, please join us for our next Multi-Omics ONLINE webinar series. This webinar series is a 3-part exploration of some of the most promising developments in multi-omics happening right now.

Week in Brief: Week Ending 23rd August

Happy Monday everybody – we hope you’re enjoying the long weekend! As usual, we’ve got the latest stories from the […]

Enhancing variant interpretation: Obtaining answers from a vast universe of data 

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, easier and more efficient? In this webinar, we will demonstrate how variant interpretation software can improve the accuracy and speed of variant interpretation, using specific case studies, such as detecting compound heterozygous variants in Charcot-Marie-Tooth Disease, and Alu insertions in breast cancer.  
In these early stages of progress, clear and informative dialogue between experts in the field is vital. No one has the time to read all the papers and preprints necessary to truly ‘stay ahead’. Therefore, a tailored webinar series such as this is the perfect opportunity to learn on the go. 

So, please join us for our next Multi-Omics ONLINE webinar series. This webinar series is a 3-part exploration of some of the most promising developments in multi-omics happening right now.

Genomics Week in Brief: Week Ending 7th June

Happy Monday everyone! We’re back with Week in Brief, your stop for the latest news from the genomics world. There […]

World of Genomics: Zimbabwe

Article written by Bethany Hanson, Science Communications Writer. We’re heading to Southern Africa in this week’s World of Genomics, visiting […]

Conservation Genomics: Saving a Million Species from Extinction 

Conservation genomics is a new and emerging field of research that harnesses the power of genomic technology to preserve species, […]

Genomics Week in Brief: Week ending 9th September

Welcome back to Week in Brief, where we explore the latest news from the genomics world and beyond! There has […]