Single Cell RNA-Seq Realized at Scale
Evercode™ split-pool combinatorial barcoding brings a simple workflow to large-scale experiments.
Unlock Single Cell at Scale
Perform scRNA-Seq on up to 1 million cells with a single kit accommodating up to 96 different biological samples or experimental conditions.
Start pursuing uncompromising science with up to a million cells.
Consistent Quality at
Experience high gene detection and uniform results at every scale. From a pilot to a single cell atlas experiment - data quality is never compromised.
Unparalleled data quality across Evercode products - from 1,000's to millions of cells.
A Simpler Workflow
Fix cells or nuclei to lock in the biology until your experiment is ready. In timecourse studies, avoid uncertainty and remove batch bias by running samples collected on different days together.
Get Started Today – No Instrument Required
Single cell RNA-Seq is accessible in any biological lab without the hardware concerns and service contracts of previous technology generations.
We have dramatically increased throughput of high-quality single cells due to the option to fix and freeze samples with the easy-to-use fixation kits. Using Parse's kits has allowed us to sequence cell types unsuitable for microfluidics such as neurons and detect genes that were previously undetected using other single cell RNA-seq kits.
The Evercode Whole Transcriptome technology provides the reagents, software, and accessibility to pursue difficult research questions. This approach first fixes a single cell or nuclei suspension. Once fixed, the barcoding and library prep process outputs libraries ready for any Illumina sequencer. Following sequencing, our software converts data into single cell insights.
Lock in gene expression immediately after sample collection with a rapid fixation protocol. After fixation, samples can be stored for up to 6 months or proceed directly to barcoding.
Barcoding & Library PrepAppend barcodes to each transcript by progressing cells through four split-pool combinatorial barcoding steps. The kit proceeds to a standard library preparation to generate sequencing-ready molecules.
SequencingThe resulting libraries are sequenced by NGS.
Data AnalysisOur computational pipeline generates an interactive report for rapid insights. All output data files, including gene-cell count matrix, integrate seamlessly with existing open source tools such as Seurat or Scanpy.
Get the Brochure
Read more about the technology with a deeper dive into the technical details.Download brochure
Explore the Sample Data
Review the Evercode Whole Transcriptome data from a species mixing experiment, immune profiling in PBMCs, or nuclei from embryonic mouse brain.Explore sample data
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