Our solution takes you from single cell or single-nuclei suspension through library prep and sequencing and delivers immediate results via our analysis software, Trailmaker.
Unparalleled accessibility and scale for single cell research. Up to 5 million cells and 384 samples in a single experiment.
Our user-friendly platform simplifies scRNA-seq data analysis, making it accessible and transparent for researchers.
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Discover scalable, instrument-free single cell sequencing technology from Parse Bioscience
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Providing researchers single cell sequencing with unprecedented scale and ease
About ParseOur solution takes you from single cell or single-nuclei suspension through library prep and sequencing and delivers immediate results via our analysis software, Trailmaker.
Unparalleled accessibility and scale for single cell research. Up to 5 million cells and 384 samples in a single experiment.
Our user-friendly platform simplifies scRNA-seq data analysis, making it accessible and transparent for researchers.
Parse never rests. We are out in the world, at meetings and symposia, as well as presenting or participating in webinars. We would love to connect with you, answer questions, and talk about your research.

Join the nearly half a million neuroscientists from around the world who have propelled their careers by presenting an abstract at an SfN annual meeting — the premier global neuroscience event.

It’s the world’s premier hematology event, gathering over 30,000 professionals to present the latest scientific research, discuss trends, and network in the field of blood diseases.
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