Reveal More With Accurate and Scalable Long-Read Sequencing
Long-read sequencing enables the accurate identification and characterization of complex genomic features. It outperforms its short-read alternatives in de novo assembly, mapping, and variant calling applications.
Its accuracy, throughput and lower relative costs, promise to make long-read sequencing a practical solution in a broad range of genomics applications.
Download this brochure to learn more about:
- Sequencing > 10 kb fragments with greater accuracy, economy and scale
- Fully automated workflows that complete in a single day
- Reducing computing and storage costs without compromising data quality