Target Enrichment
What is Target Enrichment?
With targeted resequencing, a subset of genes or regions of the genome are isolated and sequenced. Target enrichment works by capturing genomic regions of interest by hybridization to target-specific biotinylated probes, which are then isolated by magnetic pulldown.
Illumina DNA Prep with Enrichment is the latest innovation in next-generation sequencing (NGS) target enrichment solutions. By combining bead-linked transposome-mediated tagmentation chemistry with hybrid-capture target enrichment, researchers can reduce workflow time and produce an accurate, reliable assay for target enrichment resequencing.
Benefits of NGS Target Enrichment
Hybridization-based enrichment is a useful strategy for analyzing specific genetic variants in a given sample.
Target enrichment allows researchers the ability to reliably sequence exomes or large numbers of genes (e.g. > 50 genes) using robust and straightforward workflows. It delivers dependable results across a wide range of input types and quantities. Uses include:
- Human whole-exome sequencing
- Predesigned (fixed) sequencing panels for cancer and genetic disease research
- Custom genomic sequencing
Target Enrichment vs. Other Resequencing Strategies
Hybrid capture-based target enrichment lets researchers target regions of the genome that are relevant to their specific research interests. Targeted resequencing delivers higher discovery power (ability to identify novel variants), and higher mutation resolution than PCR or Sanger sequencing.
Compared to PCR-based amplicon sequencing, hybridization-based enrichment sequencing can target a higher amount of total gene content and support more comprehensive profiling of all variant types. The larger amount of total gene content allows for the characterization of both known and novel variants for discovery-related applications.
Benefits of Target Enrichment vs. Amplicon Sequencing*
Target Enrichment |
Amplicon Sequencing |
| Larger gene content, typically > 50 genes | Smaller gene content, typically < 50 genes |
| More comprehensive profiling for all variant types | Ideal for analyzing single nucleotide variants and insertions/deletions (indels) |
| More comprehensive method, but with longer hands-on time and turnaround time** | More affordable, easier workflow |
* Data on file, Illumina 2018.
** The turnaround time is for library prep assay time (DNA to finished library).
COVID-19 NGS Solutions
NGS is uniquely positioned in an infectious disease surveillance and outbreak model. Compare target enrichment with other pathogen NGS methods such as shotgun metagenomics. Find solutions to detect SARS-CoV2, track transmission routes, study co-infection, and investigate viral evolution.
Recommended Target Enrichment Workflow
User-friendly automation-compatible workflows provide fast and flexible solutions for researchers. On-bead tagmentation chemistry enables support for a wide range of DNA input amounts, various sample sizes, and a broad range of applications.
Featured Products
NextSeq 1000 & 2000 Systems
Groundbreaking benchtop sequencers allow you to explore new discoveries across a variety of current and emerging applications, with higher efficiency and fewer restraints.
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Nextera Flex for Enrichment
A fast, integrated workflow for a wide range of applications providing targeted resequencing for custom panels, fixed panels, and whole-exome enrichment.
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BaseSpace Sequence Hub
Data management and simplified bioinformatics for labs getting started and for rapidly scaling next-generation sequencing (NGS) operations.
Learn MoreFeatured Infectious Disease Target Enrichment Solutions
Respiratory Virus Oligo Panel
Highly sensitive detection and characterization of common respiratory viruses, including SARS-CoV-2 and recent flu strains, with comprehensive, rapid target enrichment sequencing.
Respiratory Pathogen ID/AMR Panel
This NGS-based target enrichment workflow targets respiratory pathogens and antimicrobial resistance alleles, and offers simplified data analysis powered by IDbyDNA.
Related Solutions
Complex Disease Research
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Perform somatic variant profiling studies of tumor specimens.
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Investigate the protein-coding regions of the genome to uncover genetic influences on disease and population health.
Learn MoreInfectious Disease Applications
As a hypothesis-free method, NGS can distinguish between infectious disease strains that differ by as little as one SNP, and replace multiple tests.
Learn MoreSNP and SNV Genotyping
Compare techniques for detecting single nucleotide polymorphisms and variants to determine which approach is best for your needs. Learn how scientists are accelerating the ability to link variants to function and gain valuable insights into disease biology.
Additional Resources
Illumina DNA Prep Technology
Fast, integrated workflows for a wide range of applications.
Library Prep and Array Kit Selector
Find the right sequencing library preparation kit or microarray for your needs.