New Software Expands ArgenTag’s Single-Cell RNA Toolkit

We are excited to announce the release of the standalone version of our demultiplexing software, advancing our mission to make long-read single-cell sequencing more accessible to all researchers.

We continue to transform how scientists explore isoforms, alternative splicing, and cellular heterogeneity with our compact and efficient workflows. Our Single-Cell RNA Kit for Long-Read Sequencing is entirely device-free, with a wet-lab protocol of less than 5 hours. Now, researchers also have the option to process data locally. This is especially valuable for advanced single-cell users with established bioinformatics teams working with sensitive datasets.

Powered by our proprietary smart barcoding technology, the software ensures a fast and accurate cell identification—even in the presence of long-read sequencing noise—and eliminates the need for complementary short-read sequencing to generate barcode whitelists. It runs with minimal IT requirements and delivers demultiplexed data in under 12 hours. The software is fully compatible with Oxford Nanopore and PacBio sequencing platforms.

To learn more, contact your sales representative or email us at welcome@argentag.com. Our bioinformatics team will provide all the information and support you need for installation and use.

And stay tuned—we’ll soon be launching our Early Access Program for the Single-Nucleus RNA Kit for Long-Read Sequencing!