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Next-Generation Sequencing Service—Novaseq 6000 System-Illumina

The main reason for using next-generation sequencing is the effective reduction in turnaround time with NGS compared to traditional methods. At the same time, next-generation sequencing makes it possible to analyze the transcriptome and genome of a species in a detailed and holistic way. CD Genomics offers a growing range of services, from library construction to sequencing to complete experimental design and support. Our Novaseq 6000 System-Illumina-based next-generation sequencing technology can help you advance genome engineering innovation.

Name of the Instrument/Technicial Service

Novaseq 6000 System-Illumina

Introduction

Key applications for this machines are large WGS, exome sequencing, whole RNA-Seq and whole genome methylation sequencing. Four different flow cell types will be available, with ranging outputs from 1.600M up to 10.000M reads per run.
Specifications: NovaSeq 6000 System

MANUFACTURER: Illumina

Summary

The NovaSeq 6000 is a sequencing platform from Illumina that enables the sequencing of short reads with an output up to 6 Tb. The NovaSeq 6000 uses the typical Illumina sequencing workflow based on library preparation, cluster generation by in situ amplification, and sequencing by synthesis. Flexibility is one of the major features of the NovaSeq 6000. Several types of sequencing kits coupled with dual flow cell mode enable high scalability of sequencing outputs to match a wide range of applications from complete genome sequencing to metagenomics analysis.

Important Notes

The NovaSeq 6000 Sequencing System enables scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project.

CD Genomics, as a specialist sequencing company, has a large range of sequencers in our NGS Core, including Illumina MiSeq, NovaSeq, PacBio, and more. If you require this service, please contact us directly.

For research use only, not intended for any clinical use.

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