The J. Craig Venter Institute used Sanger technology for sequencing Venter's DNA, which cost an estimated $70 million and took several years, but is now focusing its efforts on sequencing more ...

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.

Dr. Aaron Wenger tells us about SPRQ chemistry, highlighting its unique benefits and role in expanding our understanding of rare diseases.

Metagenomics Sequencing Market Metagenomics Sequencing Market Dublin, Jan. 28, 2025 (GLOBE NEWSWIRE) -- The "Metagenomics ...

UC Santa Cruz researchers showcase how long-read sequencing can diagnose rare genetic diseases in days instead of years.

Transforming Genomic Medicine with Unprecedented Speed, Accuracy, and Accessibility - PanOmiQ Sets a New Standard with ...

Oxford Nanopore Technologies PLC ( ($GB:ONT) ) has issued an update. Oxford Nanopore Technologies PLC announced a Share Incentive Plan transaction ...

Long read sequencing revealed more genetic information in cases of 42 patients with rare diseases while cutting time and cost of diagnoses.

Key Findings Enabled by PacBio Technology: Synchronized Multiomic Sequencing: For the first time, a single sequencing run provided simultaneous insights into genome, methylome, epigenome, and ...

The study demonstrates the impact of PacBio’s HiFi long-read sequencing technology in identifying genetic causes of rare diseases, illustrating the feasibility of potentially replacing multiple ...

This has made protein sequencing more complicated than gene sequencing—something that Next-Generation ... In this webinar, Linghua Wang and Jeremy Goecks will talk about technology that enables new ...

View Full Profile. Learn about our Editorial Policies. What is the biggest difference between using nanopore technology for protein sequencing versus nucleic acid sequencing? Protein sequencing is a ...