scrnaseq2 is a bioinformatics workflow to analyze single-cell data.
scrnaseq2_doc is the accompanying git repository including technical documentation on how to use scrnaseq2.
Visit the resulting website here: https://dcgc-bfx.github.io/scrnaseq2_doc/
The workflow and its documentation are being written by Katrin Sameith, Andreas Petzold and Rajinder Gupta at the DRESDEN-concept Genome Center.
If you would like to contribute to this documentation, please first create your own fork of the GitHub repository. You can then work on your fork, and once your added documentation is finalized, you can create a pull request.
If you used scrnaseq2 to analyze your data, please cite it by mentioning the DRESDEN-concept Genome Center URL "https://genomecenter.tu-dresden.de".