Our kits take you from single cell or single nuclei suspensions through sequencing straight into biological insights.
Target 100s to 1000s of genes to analyze more samples with less sequencing.
Transform single cell sequencing output into understandable results.
Parse Biosciences provides researchers with the ability to perform single cell sequencing with unprecedented scale and ease.
A Seattle-based company with the mission of accelerating progress in human health and scientific research.
Customer interviews, single cell sequencing tips and tricks, and the latest updates from Parse Biosciences.
A list of upcoming conferences and webinars we are attending.
The latest news stories and press releases from Parse Biosciences.
Explore our library of resources to learn more about Evercode technology and some applications from leading researchers.
Download publications and posters featuring the Evercode technology in single cell research.
Explore datasets covering various applications and sample types or access product details.
Watch past webinars on Evercode technology and its applications.
Information and insight for the entire range of Parse Biosciences products.
The AACR Annual Meeting is the focal point of the cancer research community, where scientists, clinicians, other health care professionals, survivors, patients, and advocates gather to share the latest advances in cancer science and medicine. Stop by booth #1202 to learn more about our Evercode TCR platform.
Parse Biosciences team members will be on hand to share information about our technology and products at this symposium that explores how the genome is regulated in the brain to support neural function and plasticity.
Parse Biosciences is happy to be a sponsor of this conference which will focus on novel wet-lab and computational approaches in single cell omics field to investigate the function of complex tissues in health and disease. Our team members will be on hand to share information about the Evercode product line and technology.
Evercode™ Whole Transcriptome products are enabling scientists to push scRNA-Seq past the limitations of previous technologies to detect more genes per cell, enabling a deeper understanding of biological function – with no capital expense of an instrument required. This also means no more rushing samples between labs or scheduling time on a shared instrument.
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