A new study shows that long-read sequencing has the potential to improve the rate of diagnosis while reducing the time to ...
But UC Santa Cruz researchers are pushing forward research on a cutting-edge alternative method, called long-read sequencing, which can provide a more comprehensive dataset for finding variation, ...
“Short-read sequencing struggles with certain kinds of sequence variants, so to better capture these, we also used long-read sequencing that reads between 5,000 and 30,000 base pairs at a time ...
Long read sequencing revealed more genetic information in cases of 42 patients with rare diseases while cutting time and cost of diagnoses.