Evercode™ WT Mega v2

1 Million Cells for Your Lab Today

Consult a Single Cell Expert

WT Mini

Learn More


Learn More

WT Mega

Expand your science or capabilities by profiling up to one million cells per experiment.

Scalable Single Cell Sequencing Without the Instrument

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.

High Throughput scRNA-Seq Achieved

Start pursuing uncompromising science with up to a million cells.

Highest number of cells available
Gene Detection

Consistent Quality at
Every Scale

Experience high gene detection and uniform results at every scale. From a pilot to a single cell atlas experiment - data quality is never compromised.

Gene detection never diminishes

Unparalleled data quality across Evercode products - from 1,000's to millions of cells (Evercode™ WT v1 results shown).

Gene Detection

A Simpler Workflow
Through Fixation

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.

Fixed samples stay ready for at least 6 months

Fixation locks in the biology to provide workflow flexibility. We checked a freshly prepared sample against the same sample stored for 6 months to prove stability of the fixation and reproducibility of the assay (Evercode™ WT v1 results shown).

A Simpler Workflow Through Fixation
No Instrument Required

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.

Elisabeth Rebboah
University of California, Irvine
The Parse Biosciences Workflow

From Bench
to Insight

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.
Parse Biosciences Process - Step 1


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.

Parse Biosciences Process - Step 2

Barcoding & Library Prep

Append 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.
Parse Biosciences Process - Step 3


The resulting libraries are sequenced by NGS.
Parse Biosciences Process - Step 4

Data Analysis

Our 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.
Parse Biosciences Brochure

Get the Brochure

Read more about the technology with a deeper dive into the technical details.

Download brochure

Explore the Sample Data

Review a collection of datasets that compare differences between Parse Biosciences v1 and v2 chemistries.

Explore sample data


Information and insight for the entire range of Parse Biosciences products.

Support Suite

Advancing Research for 400+ Labs