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Whole genome, whole exome or panel sequencing in precision oncology clinical trials

With a wealth of genomic technologies rapidly advancing with falling cost, implementing genomics into trials and routine care is becoming […]

The disadvantages to integrating genomics into clinical trials

Last week, we wrote a blog post on the benefits of integrating genomics into clinical trials, such as improved methods […]

Single Cell ONLINE – A virtual series

The human body has 40 trillion cells and roughly 200 different cell types. Amongst the diverse cell types lies incredible […]

FoG 2020 Presentation Andy Brass, University of Manchester: Reshaping Health: Digital futures and reality

Andy Brass is Professor of Bioinformatics at the University of Manchester. He has worked closely with Health Education England and […]

All Wales, All the way!

Megan Fealey, NovaSeq Implementation Lead, and Joseph Halstead, Bioinformatician, from All Wales Medical Genomics Service (AWMGS) joined us to discuss […]

Biology at High Resolution – Advances in Single Cell Analysis: A Review

After being voted Nature’s ‘Method of the Year’ in 2013 and 2019, it is not surprising that researchers are increasingly […]

Women in genetics

Can you name a female scientist? For many people reading this, this may seem like a very easy question to […]

Human Genome Project: Triumph or failure?

It has been 20 years since the first draft of the human genome was unveiled. The ambitious project to sequence […]

Deep learning in genomics – are we there yet?

As genomic sequencing becomes more routine, handling the sheer volume of data being produced is causing major issues. We must […]

100kb into the genome – a quest to improve target enrichment

*** This post was written by Dr. Anja Brunner, science writer (Science Inbound) Armed with a decade of experience in […]