Skip to Main Content

PacBio Single Molecule Real-Time (SMRT) Sequencing System

Overview

The new Revio System provides the advantages of SMRT Sequencing and now makes it more affordable for all scientists to drive discovery with comprehensive views of genomes and transcriptomes. More information about the Revio system can be found here: PacBio Revio | Long-read sequencing at scale

What are HiFi reads?

HiFi reads are produced using circular consensus sequencing (CCS) mode on PacBio long-read systems. HiFi reads provide base-level resolution with 99.9% single-molecule read accuracy.

HiFi reads can be used across a wide range of SMRT sequencing applications, from whole genome sequencing for de novo assembly, comprehensive variant detection, epigenetic characterization, RNA sequencing and more.

How are HiFi reads generated?

Provides access to even more highly accurate long reads.

Operates in two modes:

  • circular consensus sequencing (CCS) mode to provide base-level resolution with >99% single-molecule read accuracy for the detection of all variant types from single nucleotide to structural variants.
  • using the continuous long read (CLR) sequencing mode to enable high-quality assembly of even the most complex genomes can expect half the data in reads >50 kb and the longest reads up to 175 kb.

Applications

  • Whole Genome Sequencing- De novo Genome Assembly
  • Targeted Sequencing- No Amp Targeted sequencing utilizes a CRISPR\Cas9 system
    • Eliminate PCR bias and errors
    • Sequence through entire repeat expansions with base-level resolution
    • Quantify repeat numbers in normal- and mutant-expanded alleles
    • Identify interruption sequences
    • Characterize somatic mosaicism
  • RNA Sequencing
    • Discover new genes, transcripts and alternative splicing events
    • Improve genome annotation to identify gene structure, regulatory elements, and coding regions
    • Increase the accuracy of RNA-seq quantification with isoform-level resolution
  • Epigenetics
    • Single Molecule, Real-Time (SMRT) Sequencing directly detects epigenetic modifications by measuring kinetic variation during base incorporation. By capturing these modifications simultaneously with sequence data, this method eliminates the need for special sample preparation and additional sequencing

Sample Submission

Please contact Guilin Wang or Evelyn Ng for PacBio service request.

Sample Requirements

Ensure all samples are shipped in dry ice and are clearly labeled. Pacific Biosciences recommends resuspending your samples in either water or 10 mM Tris-HCl. Please see the table and list below for additional DNA quantity and quality requirements and recommendations.

Sequencing Application

Minimum Quantity Needed (per Library)

250 bp to 3 Kb insert library preparation

250 ng - 2 µg

3 - 10 Kb insert library preparation

2 µg - 5 µg

10 - 20 Kb insert library preparation

10 µg - 20 µg

Recommended Characteristics of DNA Suitable for Single-Molecule Sequencing

  • Minimal DNA quality: OD 260/280 and OD 260/230 should be 1.8-2.0
  • Must be double-stranded. Single-stranded DNA will not be made into a SMRTcell template in the template preparation process and can interfere with quantitation and polymerase binding.
  • Has undergone a minimum of freeze-thaw cycles.
  • Has not been exposed to high temps (> 65°C for more than one hour can cause a detectable decrease in sequence quality).
  • Has not been exposed to pH extremes (< 6 or > 9).
  • Does not contain insoluble material.
  • Does not contain RNA.
  • Has not been exposed to intercalating fluorescent dyes or ultraviolet radiation.
  • Does not contain chelating agents (e.g., EDTA), divalent metal cations (e.g., Mg2+), denaturants (e.g., guanidinium salts, phenol), or detergents (e.g., heme, humic acid, polyphenols).

Service Fees

Rates as of 7/1/2024
Type of Service Yale Fee Non-Yale* Fee
PacBio Library Prep $459 $631
PacBio SMRTCell Sequencing $1,625 $2,170
PacBio IsoSeq cDNA Prep $260 $361
PacBio Kinnex library prep $918 $1,218
Data Analysis $340 $497