Illumina Sequencing

GENEWIZ offers a standalone Illumina Next Generation Sequencing service for any library type with traditional barcoding, including RNA-Seq, whole genome sequencing, ATAC-Seq, single-cell sequencing, targeted amplicon sequencing, and more. Our optimized processes, strict quality control, and extensive experience enable us to deliver accurate and trustworthy results within industry-leading turnaround times.

We combine customizable sequencing solutions with multiple data output deliverables to match the budget and timeline of your NGS project, ensuring you get the highest quality data for your research. Our expert Ph.D. scientists can accept individual or pre-pooled libraries for sequencing on multiple Illumina® platforms.

Request Quote
Promotion banner for Next Generation Sequencing services
eBook

A Guide to RNA Sequencing

An in-depth guide for achieving success in your RNA-Seq experiments

Download Now
Cover image for the eBook A Guide to RNA Sequencing

Customizable Illumina DNA Sequencing Options

  • Illumina Platforms

    NovaSeq™ X Plus
    NovaSeq™ 6000
    MiSeq™

  • Sequencing Mode

    2×150 bp
    2×250 bp
    2×300 bp

  • Data Output

    Lanes
    Flow Cells

  • Deliverables

    FASTQ files
    Quality report
    Data analysis (upon request)

See Illumina Sequencing FAQs for more information.

Illumina Sequencing Services

  • Partial Lane/Flow Cell

    Prepare your own NGS libraries and access the power of high-output platforms, like the NovaSeq X Plus, without the cost of a full lane. This service enables you to achieve cost-effective, high-throughput sequencing without compromising quality.

    Request Quote

  • Dedicated Lane/Flow Cell

    Prepare your own NGS libraries and access the power of high-output platforms, like the NovaSeq X Plus, without the cost of a full lane. This service enables you to achieve cost-effective, high-throughput sequencing without compromising quality.

    Request Quote

  • Single-Cell Sequencing Only

    Get optimized and flexible NGS for your single-cell libraries using high accuracy Illumina platforms. Designed for researchers who prepare their own single-cell libraries, this service provides high-throughput, high-fidelity sequencing with expert support and rapid turnaround.

    Request Quote

The GENEWIZ Difference

  • Highly Scalable

    Submit one or hundreds of samples

  • Fast Turnaround

    Latest Platforms

  • European Provider

    Sequencing and customer support in Leipzig, Germany and Oxford, England

  • Superior data quality with standard, single-cell, and custom libraries
  • Fast turnaround times to suit your project needs
  • Dedicated support through local study managers plus real-time project updates
  • Local language support in several European languages including English, French, German, and Spanish

Technical Resources

NGS Platforms

For information on our NGS platforms as well as recommended configurations of your projects, please visit the NGS Platforms page. GENEWIZ does not guarantee data output or quality for sequencing-only projects.