Researchers at the University of California San Diego have identified new genetic variants associated with autism spectrum disorder (ASD) by using long-read whole genome sequencing (LR-WGS), an ...
Oxford Nanopore long-read sequencing helps researchers derive insights from difficult-to-read genomic sections and detect large structural variants. However, the technique uses high molecular weight ...
The single-cell genomics industry does not stop advancing, with a steady stream of new companies, kits, acquisitions, and more. One new company, ArgenTag, was founded in Argentina during the COVID-19 ...
Pharmacogenomics (PGx) provides insights into how genetics affect drug responses. However, short-read panels can struggle to decipher the full depth of the genome. Long-read sequencing can measure ...
When we think of parasites, we picture ticks or worms. But lurking inside our own genomes are far stealthier hitchhikers: jumping fragments of human DNA that behave like genetic parasites and can ...
To celebrate its addition to PacBio’s (CA, USA) Compatible Partner Program, ArgenTag (NY, USA) has announced the opening of a grant program to provide access to single-cell sequencing tech, free of ...
Researchers at the University of California San Diego have identified new genetic variants associated with autism spectrum disorder (ASD) by using long-read whole genome sequencing (LR-WGS), an ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results