Binx Health and Sherlock Biosciences have announced a partnership to develop the world’s first point-of-care diagnostic test for COVID-19 using […]
Sequenced genomes retain a surprisingly large number of “dark” regions – sections that have proven difficult to characterise via short-read […]
Single nucleotide variants (SNVs) are implicated in about half of all genetic diseases and so, accurately targeting and editing these […]
The genetic information of a cancerous tumour is typically obtained by sequencing the tumour cells together, rather than analysing them […]
*** This post was written by Dr. Anja Brunner, science writer (Science Inbound) Armed with a decade of experience in […]
The ability to sequence a patient’s genome can be an invaluable tool in healthcare, especially as we move towards more […]
On Thursday 18th June at 4pm BST/ 11am EST, Front Line Genomics is bringing you an interactive discussion from global […]
This article has been written by our guest contributor, Alice Godden. Image credit: Freepik.com In this short feature, I […]
With a wealth of genomic technologies rapidly advancing with falling cost, implementing genomics into trials and routine care is becoming […]
Alastair Greystoke joined Newcastle University and the Northern Centre for Cancer Care, in Newcastle upon Tyne, UK, in 2014 after […]
