News
Long-read sequencing produces genomic data by generating individual reads ranging from 1,000 to 20,000 nucleotides or more in length, while most short-read sequencing technologies use fragments ...
seqWell is designated as a PacBio Compatible Partner with novel tagmentation-based workflow that improves throughput and scalability of long read assays. BEVERLY, Mass.--(BUSINESS WIRE)--seqWell ...
SNS Insider Unveils Strategic Insights into the U.S. Long Read Sequencing Market's Exponential Growth-Valued at USD 220.26 Million in 2023-While the ...
Novel long-read sequencing data approaches are presented including tools enabling genome assembly, overcoming challenges posed by repetitive regions (Chakravarty et al. 2025; Vrček et al. 2025 ...
Hosted on MSN8mon
Long-read sequencing technique helps analyze chromosomal abnormalities in complex health conditions - MSNMore information: Jesper Eisfeldt et al, A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities, Genome Research (2024). DOI: 10.1101/gr.279510.124 ...
BOSTON, June 12, 2025 /PRNewswire/ -- Volta Labs, a genomics applications company, today announced the launch of its Library Prep App for Oxford Nanopore LSK114 on the Callisto™ Sample Prep ...
Long-read sequencing technologies analyze long, continuous stretches of DNA. These methods have the potential to improve researchers' ability to detect complex genetic alterations in cancer genomes.
Long-read sequencing delivered conclusive diagnosis for 11 of the 42 patients in the cohort, providing everything that was known from the short-read data as well as additional information ...
A new study shows that long-read sequencing has the potential to improve the rate of diagnosis while reducing the time to diagnosis from years to days -- in a single test and at a much lower cost.
SAVANA: reliable analysis of somatic structural variants and copy number aberrations using long-read sequencing. Nature Methods , 2025; DOI: 10.1038/s41592-025-02708-0 Cite This Page : ...
Long-read sequencing delivered conclusive diagnosis for 11 of the 42 patients in the cohort, providing everything that was known from the short-read data as well as additional information, including ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results