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NGS Service—Pacific Biosciences RSII DNA Sequencer

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 RSII DNA Sequencer-based next-generation sequencing technology can help you advance genome engineering innovation.

Name of the Instrument/Technicial Service

Pacific Biosciences RSII DNA Sequencer

Introduction

Specifications
1. The instrument is capable of running up to 16 SMRT cells in a single run. SMRT cells are purchased in packages of 8.
2. Each SMRT cell is interrogated by creating a movie of ZMWs as incorporation occurs in real time. The movies are interpreted as base calls using software known as SMRT Analysis resulting is FASTQ data files for analysis. Movies can be from 30 mins to 6 hrs, the longer the movie the greater the average read length.
3. Average read length for the RSII is 10 to 20Kb.
4. Typical library lengths are 2Kb or less, 10Kb, 20Kb and longer. This may require the isolation of higher molecular weight DNA and shearing using mechanical means such as a syringe or G-tube.

Applications

1. This instrument was revolutionary when introduced in being a single molecule sequencer capable to long DNA sequence reads (may exceed 40Kb). This made the SRII the first long read sequencer capable of bridging large repetitive genome regions. Since its introduction a number of applications have been developed
1) Whole genome sequencing is its most significant application
2) Targeted resequencing
3) RNA sequencing
4) Epigenetics
2. For sequencing, DNA fragments of the desired length are ligated to SMRT Bell adaptors which both create a circular template and provide polymerase binding sites. Sequencing can then proceed based on the tethering of polymerase-bound DNA templates within minute pores within a SMRT cell. The incorporation of single nucleotides is then detected using optics to provide real time sequencing of individual template molecules, one for each pore (zero mode waveguide or ZMW).
3. Sequencing is done using SMRT cells which contain 150,000 ZMWs. This results in a yield of about 30,000 to 60,000 individual sequence reads per cell.

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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