NGS Service—PacBio Sequel II

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

Name of the Instrument/Technicial Service

PacBio Sequel II

MANUFACTURER: Pacific Biosciences

Summary

The PacBio Sequel II platform generates long read lengths while maintaining high consensus accuracy and unbiased coverage. The maximum read length is more than 50 kb and high fidelity (HiFi) reads > 10 kb with > 99.9% accuracy can also be generated. This platform can generate sequence reads that support high-quality assemblies from small bacterial genomes all the way up to diploid human genomes. Other applications include amplicons, full length 16s sequencing, epigenomes, and RNA isoforms. For most applications one SMRT cell generates 20-50 Gb of data and completes in 20-30 hours.

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.

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