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

Researchers at Karolinska Institutet have developed a rapid and cost-efficient sequencing method that can identify antibiotic ...

Routine newborn screening (NBS) has transformed early disease detection. However, traditional biochemical tests limit the ...

Tuberculosis (TB) is the world’s leading cause of death from a single infectious agent, affecting more than 10 million people ...

UT researchers have developed the first viable alternative to a 75-year-old method for sequencing proteins. Image of amino acids, the building blocks of proteins. Scientists at The University of Texas ...

When the COVID-19 pandemic was at its peak, and multiple variants were threatening lives around the world, scientists relied ...

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 ...

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, ...

Whole genome sequencing (WGS) is not necessarily a solution for someone with a rare, monogenic disease. Indeed, more than half of families with suspected rare monogenic diseases do not have an answer ...

A new sequencing-based method uses molecular barcodes to trace synaptic connections among neurons. The approach enables large ...