A new study published in Cell Death and Disease has revealed the role of miR-93 in tumorigenesis and chemosensitivity. Breast […]
An article published in Nature Medicine has demonstrated that a combined risk score improves type 1 diabetes (T1D) prediction in […]
Genomics England Chief Scientist, Professor Sir Mark Caulfield, recently joined BBC Radio 4 to discuss the progress of the GenOMICC […]
Autism spectrum disorder (ASD) affects one in 54 children in the US and is associated with a heritability between 50-90%. […]
A recent article published in Nature, describes a breakthrough in our knowledge of the human genome with the first gapless, […]
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 […]
A study using Electronic Medical Records and Genomics Network have tracked the frequency and type of secondary or incidental findings […]
The ability to sequence a patient’s genome can be an invaluable tool in healthcare, especially as we move towards more […]
Metastasis occurs when the cancer cells escape the original tissue and establish new tissue elsewhere. Most cancer deaths are caused […]
