Company

Technology

Discover scalable, instrument-free single cell sequencing technology from Parse Bioscience

Technology Overview


Resources

Explore our collection of resources to learn more about technology and its applications from leading researchers

Resources Overview

Company

Providing researchers single cell sequencing with unprecedented scale and ease

About Parse

Technology

Discover scalable, instrument-free single cell sequencing technology from Parse Bioscience

Technology Overview
Evercode™ Combinatorial Barcoding

Insights included with every kit

Every kit comes with our data analysis package, which helps you assess data quality, identify sample differences, and interrogate genes of interest. An interactive web report allows anyone to easily browse the data in addition to more complex downstream analysis.

Get deep with datasets

Easily convert sequencing outputs straight to processed data

Our software takes your resulting sequencing outputs and converts it directly into processed data for you to explore. It generates the cell-by-gene count matrix by mapping the barcoded reads, performs cell clustering, and calculates differential expression to inform your experimental insights. It’s also compatible with outputs from any NGS sequencing platform.

Seamless integration with popular analysis tools

Easily move your results into other single cell analysis tools to continue your exploration. We provide tutorials for integrating the output gene count matrix files with third-party tools, such as Seurat, Scanpy, and cellxgene, to facilitate research in your platform of preference.

Parse secondary analysis in Seurat and more

Interactive results

The data analysis pipeline translates the sequencing outputs into an interactive report that allows you to immediately start exploring your data. Understand key metrics, how your cells cluster, and which cells express your genes of interest.

Easily convert sequencing outputs straight to processed data

Our software takes your resulting sequencing outputs and converts it directly into processed data for you to explore. It generates the cell-by-gene count matrix by mapping the barcoded reads, performs cell clustering, and calculates differential expression to inform your experimental insights. It’s also compatible with outputs from any NGS sequencing platform.

Seamless integration with popular analysis tools

Easily move your results into other single cell analysis tools to continue your exploration. We provide tutorials for integrating the output gene count matrix files with third-party tools, such as Seurat, Scanpy, and cellxgene, to facilitate research in your platform of preference.

Parse secondary analysis in Seurat and more

Interactive results

The data analysis pipeline translates the sequencing outputs into an interactive report that allows you to immediately start exploring your data.

Understand key metrics, how your cells cluster, and which cells express your genes of interest.