Illumina Complete Long Read Pre, Human: Unveiling the Human Genome with Unprecedented Detail
Embark on a revolutionary journey into the human genome with the Illumina Complete Long Read Pre, Human from the Genetic Disease Kits by Illumina. This cutting-edge solution transcends traditional genetic analysis, offering an unparalleled glimpse into the intricate complexities of the human genetic code.
From unraveling complex genetic disorders to understanding population-level genomic variations, this kit is a versatile instrument for a myriad of genomic research applications. It’s not just about sequencing; it’s about pushing the boundaries of what we know about the human genetic landscape.
Unprecedented Genetic Detail:
The Complete Long Read Pre, Human isn’t just a genetic test; it’s a portal to unparalleled detail. With extended read lengths, this kit captures genetic information with an unprecedented level of granularity, revealing intricacies that were once hidden.
Comprehensive Genome Exploration:
Illuminate the dark corners of the human genome. This kit is designed for comprehensive genome exploration, uncovering structural variations, complex regions, and other elusive genetic elements that standard sequencing may miss.
Advancing Genomic Understanding:
Propel your genomic research forward. The Complete Long Read Pre, Human equips researchers with the tools to delve into previously uncharted territories, fostering discoveries that contribute to our evolving understanding of the human genome.
- Genomic DNA Samples
This kit’s compatibility with genomic DNA samples ensures a seamless integration into your research workflow, providing researchers with flexibility and ease of use.
Streamline, 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