NGS Service—Illumina NovaSeq 6000 System

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 Illumina NovaSeq 6000 System-based next-generation sequencing technology can help you advance genome engineering innovation.

Name of the Instrument/Technicial Service

Illumina NovaSeq 6000 System

Introduction

1. Run Time: ~13 hr - ~44 hr
2. Maximum Output: 6 Tb
3. Maximum Reads per Run: 20 billion single-end reads; 40 billion paired-end reads
4. Maximum Read Length: 2 × 250 bp
5. DRAGEN Data Analysis Offerings:
1) (on-premise or cloud)
2) DRAGEN Germline
3) DRAGEN Enrichment
4) DRAGEN Somatic

MANUFACTURER: Illumina

Summary

The NovaSeq 6000 Sequencing System is designed to adapt to your needs. This robust, scalable system has been adopted by leading research centers and featured in countless publications. Impactful discoveries are within reach.

Applications

1. Whole-genome sequencing
2. Whole-exome sequencing
3. Whole-transcriptome sequencing

Service Features

1. Scalable throughput
2. Flexible configurations for broad, deep sequencing
3. Streamlined operations and automated flow cell loading
4. Automation-friendly

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

Please fill out the form below and we will get back to you as soon as possible with a quotation for the item you are interested in.