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

    NGS workflow basics Next-generation sequencing involves four basic steps: extraction, library preparation, sequencing, and data analysis.

  2. Coronavirus Sequencing | NGS for COVID-19 (SARS-CoV-2

    NGS can identify novel coronavirus variants, track COVID-19 transmission, and more. Compare NGS methods for various coronavirus sequencing goals.

  3. 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.

  4. Methylation Sequencing | NGS advantages - Illumina

    In this eBook, discover the value of sequencing both genetic variants and DNA methylation, together, to unravel the mechanisms of genetic disease, cancer, and other complex diseases.

  5. Next-generation Sequencing for Beginners | NGS basics for …

    The basic next-generation sequencing process includes fragmenting DNA/RNA into multiple pieces, adding adapters, sequencing the libraries, and reassembling them to form a genomic …

  6. Shotgun metagenomics: a next-generation sequencing approach that allows researchers to comprehensively sample all genes of all organisms present within a complex sample.

  7. Proteomics | Profile the proteome with NGS - Illumina

    Just as next-generation sequencing (NGS) revolutionized genomics and transcriptomics with unprecedented speed, accuracy, and scalability, this technology is now being applied to study …

  8. NGS Workflow Steps | Illumina sequencing workflow

    The next-generation sequencing workflow contains three basic steps: library preparation, sequencing, and data analysis.

  9. Long-Read Sequencing Technology | For challenging genomes

    Long-read sequencing can help resolve challenging regions of the genome, detect complex structural variants, and facilitate de novo assembly.

  10. Sample Multiplexing | Multiplex sequencing with indexes

    With multiplex sequencing, individual "barcode" sequences are added to each DNA fragment during next-generation sequencing (NGS) library preparation so that each read can be …