Next-Generation Sequencing Service—NextSeq 500

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 NextSeq 500-based next-generation sequencing technology can help you advance genome engineering innovation.

Name of the Instrument/Technicial Service

NextSeq 500

Introduction

The NextSeq500 supports a broad range of sequencing applications and offers tunable read length (75 bp, 150 bp and 300 bp) and multiple output configurations providing up to 400 million reads for pair-end sequencing runs. Additionally, the NextSeq500 is fully integrated with BaseSpace to simplify data sharing in the cloud.

Summary

The NextSeq 500 fast sample-to-results workflow enables rapid sequencing of exomes, whole genomes, and transcriptomes in a single run.

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.