Next-Generation Sequencing Service—Illumina NovaSeq 6000

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 BioSciences offers a growing range of services, from library construction to sequencing to complete experimental design and support. Our Illumina NovaSeq 6000-based next-generation sequencing technology can help you advance genome engineering innovation.

Name of the Instrument/Platform

Illumina NovaSeq 6000

MANUFACTURER:

Illumina

MODEL:

NovaSeq 6000

Introduction

The Illumina NovaSeq 6000 sequencing system is ideal for projects requiring a higher read depth. Multiple flow cell types and read length combinations offer flexible output and run time configurations based on project needs, offering output up to 6 Tb and 20 B reads in < 2 days.
Generated sequencing data is provided in the standard fastq file format, allowing users access to a wide range of established protocols, workflows, data sets and data analysis tools.

Feature Highlights

Scalable Throughput
The NovaSeq 6000 System offers high-throughput sequencing across a broad range of applications. Meet your research needs with unprecedented throughput at the lowest cost per sample.
Highly Flexible
The NovaSeq 6000 System provides tremendous scalability and flexibility to accommodate diverse applications and project sizes, while achieving maximum operational efficiency. Users can run 1 or 2 flow cells at a time and choose between 3 flow cell types, easily adjusting output for each sequencing run. With highly tunable data output you can run virtually any genome, sequencing method, and scale of project.
Broad Range of Applications
The NovaSeq 6000 System is compatible with a broad range of Illumina library preparation kits, from transcriptome sequencing to whole-genome sequencing and everything in between. High-quality, high-coverage sequencing offers a comprehensive view of the genome to detect variants accurately, characterize isoforms, and more. With increased throughput and reduced price per sample, the NovaSeq 6000 System is ideal for data-intensive applications.
Streamlined Operation
The NovaSeq 6000 System combines the features that make our benchtop sequencers so easy to use with the power of a high-throughput sequencing platform. It offers fully automated, onboard cluster generation to minimize hands-on time. Integrated, ready-to-use reagent cartridges streamline run setup and prevent improper loading. RFID encoded consumables enable fully automated reagent traceability. In all, it takes only minutes to set up a run on the NovaSeq 6000 System, giving you increased lab efficiency.

Summary

The NovaSeq 6000 offers scalable sequencing through multiple flow cell modules. The most cost-effective module is the S4 which produces ~2.5 Tb per flow cell or ~ 625 Gb per lane. Due to the extremely high quantity of sequence output, this technology is primarily useful for projects requiring a very large number of reads, such as whole genome, whole exome and multiplexed transcriptome experiments.

CD BioSciences, 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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