NGS Service—NovaSeq 6000

WELCOME TO CD GENOMICS

Genomics-Related Laboratory Services

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-based next-generation sequencing technology can help you advance genome engineering innovation.

Name of the Instrument/Technicial Service

NovaSeq 6000

Introduction

NovaSeq S2:
Read length: 2×100, of Clusters per lane (millions): 1650, Bases per lane (Gbp): 330
NovaSeq S2:
Read length: 2×150, of Clusters per lane (millions): 1650, Bases per lane (Gbp): 500
NovaSeq S4:
Read length: 2×150, of Clusters per lane (millions): 2000, Bases per lane (Gbp): 600

Summary

The NovaSeq 6000 further improves on Illumina's patterned flow cell technology. The dual-flow system delivers the highest throughput and lowest price per sample across multiple applications.

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.

Online Inquiry

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