The foundation to discovery and insights. Quality, precision, and ease of use in every step with our library prep portfolio advancements.
Get more out of your samples, reduce hands-on time, and save money. Benefit from the best customer support using the entire Illumina workflow.
*Specifications for Illumina DNA Prep kit. This is just one example; see chart below for specifications on other time-saving library prep kits.
Library preparation with continual innovation. The result: a workflow that is even easier to use, scalable for any size lab, requires a small number of steps, and has a fast workflow time. Breakthrough technology in our library prep helps you get to answers in less time.
Illumina library prep protocols accommodate a range of throughput needs, from lower-throughput protocols for small labs to fully automated library preparation workstations for large laboratories or genome centers. Our solutions support a broad range of sample types, from cell lines to fresh tissue, formalin-fixed paraffin-embedded (FFPE) samples, blood, and other challenging sample types.
Not only do our library preparation kits save you time and money, they are optimized specifically for our instruments and secondary analysis platform, DRAGEN. Even those new to NGS will find the workflows and applications are easy to adopt. In addition, you’ll experience superior support across the entire workflow because our customer support team will have more information to help you troubleshoot your sequencing runs.
Our partners have developed both high- and low-throughput walk-away automation methods that span our library prep portfolio.Learn More
Increase the number of samples sequenced per run and optimize high-throughput sequencing using unique dual index adapters.Learn More
Unique molecular identifiers (UMIs) provide error correction and accuracy. They can reduce false-positive variant calls while increasing variant detection sensitivity.Learn More
Learn about technology advancements and innovations that provide you with novel, easy-to-use, and fast solutions for both DNA and RNA library preparation.View Webinar
|Application||Whole-genome sequencing||Whole-genome sequencing||DNA enrichment - no UMI|
|Hands-on time||~45 min||1-1.5 hrs||~2 hrs|
|Turnaround time||~1.5 hrs||~3-4 hrs||~6.5 hrs|
|Input||25 ng to 300 ng||1 ng to 500 ng||10 ng to 100 ng|
|Automation available||Available Soon||Yes||Yes|
|Library Quant needed?||No||No||No|
|Fragmentation included?||Yes – on bead||Yes – on bead||Yes – on bead|
|Product||Illumina DNA PCR-Free Prep||Illumina DNA Prep||Illumina DNA Prep with Enrichment|
|Application||Whole transcriptome||mRNA||RNA enrichment|
|Hands-on time||< 3 hrs||< 3 hrs||< 2 hrs|
|Turnaround time||~7 hrs||6.5 hrs||< 9 hrs|
|Input||1 to 1000 ng standard quality RNA; 10 ng for optimal performance and FFPE samples||25 to 1000 ng standard quality RNA||10 ng standard quality RNA; 20 ng RNA for low quality / degraded / FFPE|
|Automation capability||Liquid handling robots||Liquid handling robots||Liquid handling robots|
|Library Quant needed?||Yes||Yes||Yes|
|Fragmentation included?||Yes||Yes||Not required|
|Product||Illumina Stranded Total RNA Prep||Illumina Stranded mRNA Prep||Illumina RNA Prep with Enrichment|
We'll walk through your needs and make recommendations.
Our innovative NGS library preparation portfolio uses three key technologies. Find out the benefits of each approach and how they differ.
This technology uses bead-bound transposomes for a more uniform reaction compared to in-solution tagmentation reactions.
The ligation process prepares NGS libraries by fragmenting a genomic DNA or cDNA sample and ligating specialized adapters to both fragment ends.
With a PCR-based workflow and ease of use for users new to NGS, amplicon library prep can measure thousands of targets simultaneously.
Find guidance to help you avoid contamination while purifying DNA/RNA before library preparation.
Learn how to convert library concentration from ng/µl to nM for some Illumina library preparation methods.
Find out how to quantify and validate final libraries for a successful sequencing run.
Learn when library normalization is required, and how to perform the necessary steps.
Learn how to use the PhiX library as a control in your Illumina sequencing runs.
Simultaneous qualification and quantification of nucleic acids with the Fragment Analyzer.