Using single-cell epigenomic profiling of immune cells from 110 individuals, researchers show that genetic variation and ...

For the first time, researchers at King's College London and the University of Florence have identified the specific genetic ...

Researchers at King's College London and the University of Florence have, for the first time, identified the specific genetic ...

The past decade has delivered landmark advances in human and medical genomics that shape how we understand disease mechanisms ...

The human genome is organised in 46 chromosomes, where all but the x and y chromosomes in men are present in two copies. This means that a person with a faulty gene on one chromosome most often has a ...

Despite the development of cutting-edge genetic testing techniques and considerable progress in our understanding of the genetic basis of idiopathic pulmonary fibrosis (IPF), missing heritability and ...

Knowing how human DNA changes over generations is essential to estimating genetic disease risks and understanding how we evolved. But some of the most changeable regions of our DNA have been ...

By integrating long-read and short-read transcriptomics with whole-genome resequencing, the team uncovered specific transcript variants and genetic ...

Chronic traumatic encephalopathy (CTE) is a neurodegenerative disease caused by repetitive head impacts (RHI). However, individuals with similar RHI exposure have shown differing pathology, suggesting ...

Genetic variation in livestock is a critical area of research that underpins modern breeding practices and agricultural productivity. Differences in DNA sequences, including single nucleotide ...

Research into genetic variation and wool traits in sheep and goats has revealed critical insights into the structural composition and quality of animal fibres. Studies have focused on ...