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.
Pair guide RNAs with single cell whole transcriptomes.
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.
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Evercode™ split pool combinatorial barcoding technology converts each cell or nucleus into an individual reaction compartment. This approach steps away from the limitations of hardware-based offerings for a more elegant solution to single cell RNA sequencing (scRNA-seq) and single nuclei RNA sequencing (snRNA-seq).
The Parse Biosciences pipeline can run locally on your own computer or in the cloud using the DNAnexus® platform. The pipeline produces standard output files (including gene-cell count matrix compatible with third-party analysis tools like Seurat and Scanpy) and an interactive HTML report that enables exploration of cell type clustering and gene expression.
Talk to our team to request a quote or plan your next experiment.
Studies increasingly require larger sample and cell numbers. Other single-cell technologies are limited by the number of samples that can be analyzed together, introducing batch effects. Evercode WT has a kit to fit any study, regardless of scale.
Increased sensitivity enables better detection of lowly expressed genes, resulting in more comprehensive annotation of cell types. Run more samples, use less sequencing, and delve deeper into the biology with gene and transcript detection that outperforms droplet-based methods.
Evercode Whole Transcriptome Technical Brochure
