Information on tumor mutational status was limited before the development of NGS because traditional Sanger sequencing and ...

Genetic sequencing has gone through several advances. A major breakthrough came when scientists began breaking the billions ...

Published in Cell, the study titled, “Long somatic DNA-repeat expansion drives neurodegeneration in Huntington’s disease,” ...

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 ...

Scientists unveil the androgen clock, a precise epigenetic tool to measure long-term androgen exposure and its role in aging ...

What may be the first commercially available book saved in DNA is the latest example of how consumers might use molecular ...

Within a few days of being born, more than 300,000 Australian babies a year have a spot of their blood analyzed to screen for ...

Study explains long-standing question of why Huntington’s disease symptoms typically do not appear until midlife even though ...

Scientists at the Broad Institute of MIT and Harvard, Harvard Medical School, and McLean Hospital have discovered a ...

Understanding biological relationships is often critical when studying animal populations. Researchers have now developed a transformative approach that identifies stretches of DNA that two ...

Past psychology research suggests that there is a strong relationship between difficult experiences during childhood and the ...

T CDx is a 648-gene next-generation sequencing test for solid tumor profiling, which includes microsatellite instability status and companion diagnostic claims for colorectal cancer patients. xT CDx ...