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

Fast, Flexible Sequencing

Plug and Play into Existing Lab Ecosystems

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.


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


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


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


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


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


Accurate whole-exome sequencing with high concordance, coverage depth, and uniformity.
Sequencing on G4X
Flow Cell
Config.1
# REads2
Run Time3
Quality4
2Indicates typical paired reads passing filter. Throughput may vary depending on application and read length.
3Sequencing run time includes analysis time, and is measured from run start through clustering, sequencing, and instrument wash for non-indexed reads. Run time will vary depending on the number of flow cells and the high-performance computing configuration.
4Performance metrics may be impacted by application, sample quality, library preparation, loading concentration, and other sequencing considerations. Metrics as generated on Salmonella and PhiX control libraries.
Note: G4X is currently in development. Specifications, configurations, and capabilities are subject to change. Please contact us for the latest updates on availability and performance.
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REsources

Library Prep
Demo Data
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Meet with our team to discuss becoming an early G4X site.
