Scientists might have succeeded in sequencing the entire human genome, but that doesn’t mean they aren’t still learning new ...

Knowing how human DNA changes over generations is essential to estimating genetic disease risks and understanding how we ...

The scientists used a combination of short- and long-read sequencing data to assemble and analyze genomes from 28 members of the same family.

Johns Hopkins Medicine scientists say they have found a pattern of so-called epigenetic "marks" in a transition state between normal and pancreatic cancer cells in mice, and that the normal cells may ...

A genomic study of gut microbes during antibiotic use finds selective sweeps in a DNA gyrase gene that drive resistance.

For patients with disorders such as autism and schizophrenia, mutations in the same gene could require different treatments, according to new research from Yale School of Medicine (YSM).

The risk of cancer goes up with age, in part because aging impedes the body's ability to detect and destroy cells with ...

The results, said György, “[highlight] the immense potential of gene correction as a medical technology.” “This is one of the first papers that used all [of the available] human models to correct the ...

Researchers from Children's Hospital of Philadelphia (CHOP) and the Perelman School of Medicine at the University of ...

RIKEN researchers have demonstrated the protective effects of a specific genetic mutation against Alzheimer's disease in ...

GenomeIndia project publishes preliminary findings from sequencing 10,000 Indian genomes, highlighting unique genetic ...