We’ve combined sample prep and library prep into one easy-to-use product, simplifying the process to create sequence-ready samples. With on-bead fragmentation, no library quantification is needed, which saves you time and increases sequencing data performance by avoiding PCR duplicates.
Illumina DNA Prep (formerly Nextera DNA Flex) simplifies the upfront DNA fragmentation process and solves other workflow challenges such as DNA extraction, DNA quantification, and library prep QC and library quantification.Watch Webinar
Our enrichment library prep yields provides > 90% on-target reads, > 95% uniformity, and low PCR duplicate rate across all Illumina sequencing systems.1 The workflow uses a single, 90-min hybridization step and as little as 10 ng input DNA. On-bead tagmentation chemistry enables support for a wide range of DNA input amounts, various sample types, and a broad range of applications.
This video overviews the process of selecting the enrichment panel options, the library prep and enrichment workflow for Illumina DNA Prep with Enrichment (formerly Nextera Flex for Enrichment) and data analysis.View Video
Ultra-deep sequencing of amplicons allows efficient variant identification and characterization. Accelerated library prep uses reduced-bias PCR and is gel-free, enabling you to prepare high-quality libraries in less than a day. Mechanical DNA fragmentation and adapter ligation.
|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 100 ng||10 ng to 100 ng|
|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|
|For Human DNA WGS||Illumina DNA PCR-Free Prep||
|For DNA WGS with low input||Illumina DNA Prep||
|For DNA enrichment without UMI||Illumina DNA Prep with Enrichment||
Bead-linked transposome tagmentation is an innovative technology used in our library preparation portfolio. On-bead tagmentation lets you get to sequence-ready libraries faster than before by simultaneously fragmenting the gDNA and adding the Illumina sequencing primers. Normalize your library without ancillary reagents or equipment. Reduce turnaround time and complexity.Learn More
The other key technology used in our NGS library prep is adapter ligation, long known for consistent, high-quality data. Libraries are prepared by fragmenting a gDNA or cDNA sample and ligating specialized adapters to both fragment ends. These adapters contain the full complement of sequencing primer hybridization sites. This eliminates the need for additional PCR steps to add the index tag and index primer sites, making the process fully automatable.Learn More
Library prep from blood, saliva, or genomic DNA that provides uniform coverage for human whole-genome sequencing (WGS).
Library prep that provides uniform coverage and improved genome assembly for viruses, bacteria, and other microbial species.
Library preparation and unique dual indexing combined with hybrid capture of exome content.
Combining exome sequencing with Illumina DNA Prep and the analytical power of DRAGEN enables simplified, efficient, highly accurate variant analysis in FFPE tumor samples.
We'll walk through your needs and make recommendations.
View illustrated schematics of NGS DNA library preparation techniques and see brief diagrams of Illumina library preparation kit protocols.View Poster
Try one of these methods or find inspiration to create your own. With a few extra processing steps, a wide range of scientific questions can be addressed.View PDF
High performance for sensitive applications such as human whole-genome sequencing.
Sequence a tumor-normal pair or germline trio using a single S1 flow cell or up to 48 genomes per run using dual S4 flow cells.
Provides secondary analysis with high-quality variant calling.
Increase the number of samples sequenced per run and optimize high-throughput sequencing using unique dual index adapters.
Unique molecular identifiers (UMIs) provide error correction and accuracy and can reduce false-positive variant calls while increasing variant detection sensitivity.
Our partners have developed both high- and low-throughput walk-away automation methods that span our library prep portfolio.
DNA sequencing can be applied to small, targeted regions or the entire genome through a variety of methods, enabling researchers to investigate and better understand health and disease.