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Genetic risk for Alzheimer’s progression differs with sex

It is well documented that the genetic risk for Alzheimer’s has a sex bias. Sex bias in Alzheimer’s Carrying a […]

First Point-of-Care Test for COVID-19 using CRISPR announced

Binx Health and Sherlock Biosciences have announced a partnership to develop the world’s first point-of-care diagnostic test for COVID-19 using […]

Webinar: Capture the dark genome – From repeat-expansions to CRISPR unintended mutations

Sequenced genomes retain a surprisingly large number of “dark” regions – sections that have proven difficult to characterise via short-read […]

Base editing outcomes predicted by machine learning model

Single nucleotide variants (SNVs) are implicated in about half of all genetic diseases and so, accurately targeting and editing these […]

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 […]