Illumina Complete Long Read Prep, Human

With Illumina Complete Long Reads technology, long-read sequencing is now accessible and streamlined for genomic labs. Illumina Complete Long Read Prep, Human is the first product to utilize this technology, providing the most comprehensive view of the genome. The high-performance whole-genome sequencing assay uses a standard NGS workflow to generate contiguous long-read sequences on the NovaSeq 6000 System and NovaSeq X Series.

• Streamlined, accessible assay with long and short reads on a single platform, compatible wth the NovaSeq X Series and NovaSeq 6000 System
• Optimized standard NGS library prep and DRAGEN secondary analysis for highly accurate, reliable results
• Robust and flexible performance with low input requirements, no specialized extraction, shearing, or size selection required
• Efficient, single-day, automation-friendly workflow that is more scalable than on-market long-read solutions

Highly accurate, scalable assay

Illumina Complete Long Read data complements standard short-read WGS data and delivers more comprehensive whole genomes by:

• Calling variants in challenging, difficult-to-map regions with high homology or repetitive regions
• Resolving complex structural variants, pseudogenes, and large insertion–deletions (indels)
• Phasing variants and calling haplotypes