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Single-cell copy number profiling unveils the genetic diversity of cancer

The genetic information of a cancerous tumour is typically obtained by sequencing the tumour cells together, rather than analysing them […]

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 […]

A look inside a rapid exome sequencing lab

The ability to sequence a patient’s genome can be an invaluable tool in healthcare, especially as we move towards more […]

Synthetic biology in the fight against COVID-19

On Thursday 18th June at 4pm BST/ 11am EST, Front Line Genomics is bringing you an interactive discussion from global […]

Biohacking by mail order: Reckless or educational?

  This article has been written by our guest contributor, Alice Godden. Image credit: Freepik.com In this short feature, I […]

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 […]

Interview with Alastair Greystoke, Senior Lecturer & Honorary Consultant, Newcastle Hospitals Trust

Alastair Greystoke joined Newcastle University and the Northern Centre for Cancer Care, in Newcastle upon Tyne, UK, in 2014 after […]

New single-cell sperm sequencing method uncovers insights into meiotic variation

A new method has allowed researchers at Harvard Medical School to examine variation in meiosis by studying tens of thousands […]

Reverse genetics allows mapping of SARS-CoV-2 in the body

A new study accepted by Cell showed that SARS-CoV-2 infects the nasal cavity to the greatest degree and infects and […]

Opinion: We should address genetic data governance as we fight to find a COVID-19 vaccine

As the world rushes to develop a vaccine against COVID-19, geneticists are looking at our genes to understand the variation […]