Illumina 5-base solution for methylation and variant detection
Receive your quote directly from the manufacturer.
The Illumina 5-base solution provides a streamlined, end-to-end NGS library prep and analysis workflow for simultaneous methylation profiling and high-accuracy genetic variant calling.
For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).
Submicron resolution and high sample throughput deliver exceptional data quality and rapid scan times.
The NovaSeq X and NovaSeq X Plus Sequencing Systems deliver extraordinary throughput and accuracy to perform data-intensive applications at production scale.
Expansive application breadth and operational simplicity with proven performance
A complete targeted resequencing solution for a wide range of applications, with fast integrated workflow and options for custom and fixed enrichment panels.
A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.
Scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project.
An efficient, fast, and integrated library preparation workflow that yields highly accurate data for sensitive sequencing applications.
