4000 Mason Rd

Suite 304

Seattle, Washington 98195

  • White LinkedIn Icon
  • White Facebook Icon
  • White Twitter Icon

© 2019 Split Biosciences, Inc. All Rights Reserved


Single Cell Whole Transcriptome

100,000 cells and 48 samples with a single kit

Based on the principles of the academic method SPLiT-seq, Split Bio’s Whole Transcriptome kit provides the most scalable single cell RNA-seq solution on the market. Dramatic increases in transcript detection from the original academic method allow you to capture more information with less sequencing while maintaining low doublet rates.


Early Access

Split Bio is accepting a limited number of research groups to enroll as part of an early access program. Participants will be able to purchase a single cell whole transcriptome kit and receive support from the Split Bio team. Let us know if you are interested and want to learn more.

Kit workflow 


Following sample extraction, fix your single cell or single nuclei suspension(s) with a 30-60 minute protocol. After fixation your samples can be stored for up to 6 months or you can proceed directly to cell barcoding.

Cell Barcoding

Load your fixed samples (1-48) and pass cells through four split-pool combinatorial barcoding steps to append a cell-specific combination of DNA barcodes to each transcript. 


Library Prep

Prepare barcoded molecules for next generation sequencing. Up to 8 sequencing libraries (each containing 100-12,500 cells) can be prepared in parallel. Libraries can be sequenced independently at different sequencing depths.


Data Analysis

After sequencing, use our computational pipeline to generate an experimental report along with processed data (including gene-cell count matrix) that integrates into existing open source tools (Seurat, Scanpy, etc.).