In a single experiment, scientists can decipher the entire genomes of many patient samples, animal models, or cultured cells.

Genetic variants that cause rare disorders may remain elusive even after expansive testing, such as exome sequencing. The diagnostic yield of genome sequencing, particularly after a negative ...

An ambitious plan to sequence genomes for 1.85 million eukaryotic species on our planet is underway. It's a massive undertaking that will dramatically enhance our understanding of biology, and inform ...

PacBio has announced a new study published in Nature Communications that presents an innovative method for analyzing complex regions of the human genome, particularly segmental duplications that have ...

Studying endangered animal species without disturbing them and disrupting their natural habitat could be highly advantageous, ...

Cornell researchers have found that a new DNA sequencing technology can be used to study how transposons move within and bind to the genome. Transposons play critical roles in immune response, ...

Researchers have refined a powerful DNA sequencing tool that can uncover hidden mutations that occur naturally in our bodies as we age. In the largest study to date, they have used the tool to provide ...

An international team led by researchers from the Yong Loo Lin School of Medicine, National University of Singapore (NUS ...

A team of researchers has built a new protein sequencing workflow that pairs mirror proteases with deep learning software to read peptide sequences with far greater accuracy than previous methods.