Binx Health and Sherlock Biosciences have announced a partnership to develop the world’s first point-of-care diagnostic test for COVID-19 using […]
In this episode of the Genetics Unzipped podcast, supported by the UK Medical Research Council, Kat Arney and stay-at-home roving […]
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 […]
A new single-cell analysis study of airway samples of COVID-19 patients has found that drugs targeting chemokine receptors may be […]
Damage to the DNA in cells is the root cause of cancer, but it is also a weakness of the […]
As genomic sequencing becomes more routine, handling the sheer volume of data being produced is causing major issues. We must […]
A study using Electronic Medical Records and Genomics Network have tracked the frequency and type of secondary or incidental findings […]
Yesterday, 10x Genomics revealed the first 45 members chosen to participate in its Visium Clinical Translational Research Network (CTRN). The […]
