Australia’s screening program – which reaches about 99% of newborn babies – mainly uses tests that measure the levels of ...
The newly unveiled database showcases the genome sequences of healthy individuals from 99 ethnic populations of the country, ...
The cause of rare diseases is increasingly being detected through genome sequencing, which involves reading the entire human DNA by first breaking it into small pieces -- short reads. Scientists found ...
The Fortune 500 pharma giant will sequence the exomes of 10 million people, with the goal of developing new therapies and ...
Study explains long-standing question of why Huntington’s disease symptoms typically do not appear until midlife even though ...
The reappearance of the rare fish provides an opportunity for conservation efforts.
Understanding biological relationships is often critical when studying animal populations. Researchers have now developed a transformative approach that identifies stretches of DNA that two ...