Whole genome sequencing (WGS) is a pivotal tool in the research of rare diseases, providing molecular clarity for research in targeted therapies and precision medicine. In this poster, we present the use of the AVITI™ system in high-throughput WGS and large insert sequencing applications, demonstrating the flexibility and ability to scale large throughput applications with a benchtop sequencer.
Download this poster to learn how:
- High-plexity initial pool runs improve reproducibility, reduce sample requeues, and allow for sample QC.
- Large insert library preps increase benchmarking performance while maintaining high quality.
- Rapid mode sequencing improves the time to data without compromising quality.