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 Pacific Biosciences Sequel System-based next-generation sequencing technology can help you advance genome engineering innovation.
The new Sequel System is based on our proven Single Molecule, Real-Time (SMRT) Sequencing technology utilized by the RSII. Sequel SMRT Cells contain 1 million zero-mode waveguides delivering up to 10 billion bases of long-read sequence per whole-genome analysis run, and up to 20 Gb in RNA isoform sequencing (Iso-Seq).
The Sequel System is ideal for rapid and cost-effective de novo genome assembly, structural variation analysis, gene annotation, targeted analysis, and much more.
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.
For research use only, not intended for any clinical use.
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