llumina Unique Dual Indexes, LT (48 Indexes, 48 Samples)
20098166
Illumina Complete Long Read DRAGEN Cloud Analysis
20100421
Illumina Complete Long Read Prep, Human - 24, S4 starter pack
20099754
Illumina Complete Long Read Prep, Human - 24, 10B starter pack
20099755
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.
Illumina Complete Long Read data complements standard short-read WGS data and delivers more comprehensive whole genomes by:
This novel technology will bright more light to even the darkest corners of the genome. Illumina Complete Long Reads helps resolve the most challenging regions of the genome and makes long-read sequencing accessible and streamlined by enabling short and long reads from a single platform.
View VideoInstrument | Recommended Number of Samples | Read Length |
---|---|---|
NovaSeq 6000 System | 4 samples (1 sample per lane of an S4 flow cell). 8 samples (1 sample per lane of an S4 flow cell, dual flow cell run optional). A paired PCR-free WGS library is required for analysis (Illumina DNA PCR-Free Prep recommended). NovaSeq 6000 Xp Workflow kit. |
2 × 150 bp |
NovaSeq X System | 4 samples (1 sample per 2 lanes of a 10B flow cell). A paired PCR-free WGS library is required for analysis (Illumina DNA PCR-Free Prep recommended). |
2 × 150 bp |
NovaSeq X Plus System | 8 samples (1 sample per 2 lanes of a 10B flow cell, dual flow cell run). A paired PCR-free WGS library is required for analysis (Illumina DNA PCR-Free Prep recommended). |
2 × 150 bp |
In this presentation, we share use cases of Complete Long Reads and highlight research being done by collaborators around the world.
Watch on-demand webinarIllumina Complete Long Read technology will accelerate access to the remaining ~5% of genic regions. Hear Andrew Shaver, Product Manager describe the benefits of the Illumina novel long-read technology, including the accuracy, scalability, and workflow benefits. See how the Illumina Complete Long Read technology complements the technical innovations in our Illumina product portfolio.
Watch on-demand webinarTechnical Note | PDF | 8 versions
Data Sheet | PDF | 8 versions
Illumina Complete Long Read Prep Product Documentation
DRAGEN ICLR WGS (Illumina Complete Long Reads) Online Help Documentation
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Speak with one of our specialists about how your workflow and analysis can benefit from the accuracy and scalability of our long-read technology. Fill out the form to request a quote for ordering today.
* Sequencing Illumina Complete Long Read libraries on NovaSeq platforms may cause the reported Q30 score of a run to fall below the NovaSeq specification. This does not indicate a performance issue with the sequencing run, nor the library.