Accelerating clinical research with streamlined, high-throughput whole-genome nanopore sequencing
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Overview
The analysis of large cohorts of clinical research samples is critical to advancing our understanding of the mechanisms of disease and identifying novel biomarkers. Nanopore technology enables the capture of single nucleotide variants (SNVs), structural variants (SVs), copy number variants (CNVs), short tandem repeat (STR) expansions, and methylation within a single sequencing run.
This end-to-end workflow provides a scalable solution for genome-wide analysis of genomic and epigenomic variants across a large cohort of human research samples.
In this workflow overview, you will:
- Find out how nanopore sequencing reads of unrestricted length enhance population genomic applications
- Discover our best practice sequencing workflow in detail, starting from the recommended extraction method, through to primary analysis
- Learn about our recommended sequencing kit and devices