NGS Service—Illumina NextSeq500

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 NextSeq500-based next-generation sequencing technology can help you advance genome engineering innovation.

Name of the Instrument/Technicial Service

Illumina NextSeq500

Introduction

This instrument is used for sequencing DNA or RNA libraries to detect genomic variants in any organism. It can be used to detect single nucleotide polymorphisms (SNPs), insertions and deletions (INDELS), gene duplication events, and chromosomal rearrangements. Additionally, sequencing total RNA, small RNA, or mRNA can reveal information about gene expression levels, presence/absence of gene expression, gene splice variants, gene fusion events, and SNPs.

MANUFACTURER: Illumina

Summary

Sequencing Rates per run. All pricing includes kits and total number of sequencing hours required per run. This instrument is used after DNA or RNA have been converted to NGS libraries at the core.
Sequencing menu
1. NGS-High Output 300 cycles
2. NGS-High Output 150 cycles
3. NGS-High Output 75 cycles
4. NGS-Mid Output 300 cycles
5. NGS-High Output 150 cycles

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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