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  1. Next-Generation Sequencing (NGS) | Explore the technology

    Discover the broad range of experiments you can perform with next-generation sequencing, and find out how Illumina NGS works.

  2. NGS for Beginners | Learn the basics of NGS - Illumina

    These educational resources cover key topics in next-generation sequencing designed for beginners.

  3. NGS Workflow Steps | Illumina sequencing workflow

    This e-book outlines the NGS analysis workflow and provides an overview of Illumina Connected Software solutions available for analyzing gene expression and regulation data.

  4. sequencing run—nearly a 1000× increase in four years. With the ability to rapidly generate large volumes of sequencing data, NGS enables researchers to move quickly fro an idea to full data …

  5. Sequencing Platforms | Illumina NGS platforms

    Compare next-generation sequencing (NGS) platforms by application, throughput, and other key specs.

  6. NGS & Microarray Training | Hands-on or online Illumina training

    Get hands-on next-generation sequencing (NGS) or microarray training led by a certified Illumina instructor, provided at your own lab or an Illumina Solutions Center.

  7. NGS Tutorials | Bioinformatics tutorials and more - Illumina

    These next-generation sequencing (NGS) tutorials are designed to help you understand key concepts in NGS. With videos, online training, and technical bulletins, we’ll guide you through …

  8. Sequencing | Key methods and uses - Illumina

    Considering bringing next-generation sequencing to your lab, but unsure where to start? These resources cover key topics in NGS and are designed to help you plan your first experiment.

  9. Sequencing Services | NGS & whole-genome service providers

    Our NGS service offerings range from whole-genome sequencing services to oncology, noninvasive prenatal testing services, and more. We have years of experience with proven …

  10. Sequencing Coverage for NGS Experiments - Illumina

    Next-generation sequencing (NGS) coverage describes the average number of reads that align to, or "cover," known reference bases. The sequencing coverage level often determines whether …