Sequencing on G4X

Beyond spatial, G4X is also the industry's most powerful benchtop sequencer. Providing fast, flexible NGS results across sample types.

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Features

Fast, Flexible Sequencing

Daily Runs
Innovative high-speed imaging, rapid fluidics and novel chemistry work in concert to reduce run times from days to hours (under 24 hour runs across applications).
Flexible Run Sizes
Run 1, 2, 3 or 4 flow cells at a time to efficiently match run output with project requirements.
User Friendly Operation
Simple experiment management with 4 fluidically independent lanes per flow cell and tolerant to low complexity libraries and variable loading conditions.
Accurate Results
Proprietary 4-color Rapid SBS chemistry with novel nucleotides, specifically-engineered enzymes, and molecular biology methods to deliver accurate paired-read sequencing (85% bases ≥ Q30).
    Workflow

    Plug and Play into Existing Lab Ecosystems

    Compatible with a Wide Range of Library Prep Methods
    Supports diverse workflows, including leading commercial and custom library prep kits, enabling broad application flexibility across research and clinical settings.
    Simple and Intuitive Run Initiation
    User-friendly software interface enables streamlined setup with minimal steps, allowing for fast onboarding and consistent execution across users and sites.
    Effortless Bioinformatics Integration
    Standard FASTQ output ensures plug-and-play compatibility with existing pipelines, accelerating downstream analysis and minimizing data handling complexity.
      Application Performance

      Accurate Results Across Key Applictions

      Sequencing on the G4X is compatible with a wide range of sample preparation workflows, through seamless integration into bioinformatic pipelines, the G4 is a plug-and-play solution.

      Whole Genome
      High accuracy, broad variant detection
      Whole Genome Sequencing

      Accurate whole-genome sequencing with high coverage, base quality, and variant concordance.

      Targeted Somatic
      Sensitive and precise variant detection
      Targeted Sequencing

      Rapid somatic variant detection with high concordance, sensitivity, and variant calling performance.

      Single-Cell Seq
      Sensitive single-cell gene expression
      Single Cell Sequencing

      Sensitive and consistent single-cell RNA-Seq with strong gene detection.

      Bulk RNA-Seq
      Consistent performance across expression studies
      Bulk RNA-Seq

      High performance for RNA-Seq: reproducibility, coverage uniformity, transcript detection.

      Metagenomics
      Reliable detection across complex microbial samples
      Metagenomics

      High-quality microbial whole-genome sequencing with strong coverage and read depth

      Whole Exome
      High coverage and uniformity for exome panels
      Whole Exome Sequencing

      Accurate whole-exome sequencing with high concordance, coverage depth, and uniformity.

      Specifications

      Sequencing on G4X

      Flow Cell
      Config.1
      # REads2
      Run Time3
      Quality4
      F3
      100 Cycles
      300 Cycles (2x150)
      100M / Lane
      400M / FC
      1.6B / Run
      12-24 Hours
      85% ≥ Q30

      Learn More

      REsources

      Sequencing Support Hub
      Learn more about about sequencing on the G4X with detailed infomation around library preparation, kit configurations, instrument operations and analysis.

      Library Prep

      Explore compatibility of G4X Sequencing with our library prep partners

      Demo Data

      Download raw G4X sequencing data across applications

      Speak to an Expert

      Schedule a technical seminar and get your questions answered.

      Get Started

      G4X Platform Adoption

      Meet with our team to discuss becoming an early G4X site.

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