scvi-tools (single-cell variational inference tools) is a package for probabilistic modeling and analysis of single-cell omics data, built on top of PyTorch and AnnData.
scvi-tools is composed of models that can perform one or more tasks in single-cell omics data analysis. scvi-tools currently hosts implementations of:
- scVI for analysis of single-cell RNA-seq data, as well as its improved differential expression framework.
- scANVI for cell annotation of scRNA-seq data using semi-labeled examples.
- totalVI for analysis of CITE-seq data.
- gimVI for imputation of missing genes in spatial transcriptomics from scRNA-seq data.
- AutoZI for assessing gene-specific levels of zero-inflation in scRNA-seq data.
- LDVAE for an interpretable linear factor model version of scVI.
- Stereoscope for deconvolution of spatial transcriptomics data.
- DestVI for multi-resolution deconvolution of spatial transcriptomics data.
- peakVI for analysis of scATAC-seq data.
- scArches for transfer learning from one single-cell atlas to a query dataset (currently supports scVI, scANVI and TotalVI).
- CellAssign for reference-based annotation of scRNA-seq data.
- Solo for doublet detection in scRNA-seq data.
All these implementations have a high-level API that interacts with scanpy, standard save/load functions, and support GPU acceleration.
scvi-tools contains the building blocks to develop and deploy novel probablistic models. These building blocks are powered by popular probabilistic and machine learning frameworks such as PyTorch Lightning and Pyro. For an overview of how the scvi-tools package is structured, you may refer to this page.
We recommend checking out the skeleton repository as a starting point for developing and deploying new models with scvi-tools.
For conda,
conda install scvi-tools -c conda-forge
and for pip,
pip install scvi-tools
Please be sure to install a version of PyTorch that is compatible with your GPU (if applicable).
- Tutorials, API reference, and installation guides are available in the documentation.
- For discussion of usage, check out our forum.
- Please use the issues to submit bug reports.
- If you'd like to contribute, check out our contributing guide.
- If you find a model useful for your research, please consider citing the corresponding publication (linked above).
If you used scvi-tools in your research, please consider citing
@article{Gayoso2022,
author={Gayoso, Adam and Lopez, Romain and Xing, Galen and Boyeau, Pierre and Valiollah Pour Amiri, Valeh and Hong, Justin and Wu, Katherine and Jayasuriya, Michael and Mehlman, Edouard and Langevin, Maxime and Liu, Yining and Samaran, Jules and Misrachi, Gabriel and Nazaret, Achille and Clivio, Oscar and Xu, Chenling and Ashuach, Tal and Gabitto, Mariano and Lotfollahi, Mohammad and Svensson, Valentine and da Veiga Beltrame, Eduardo and Kleshchevnikov, Vitalii and Talavera-L{\'o}pez, Carlos and Pachter, Lior and Theis, Fabian J. and Streets, Aaron and Jordan, Michael I. and Regier, Jeffrey and Yosef, Nir},
title={A Python library for probabilistic analysis of single-cell omics data},
journal={Nature Biotechnology},
year={2022},
month={Feb},
day={07},
issn={1546-1696},
doi={10.1038/s41587-021-01206-w},
url={https://doi.org/10.1038/s41587-021-01206-w}
}
along with the publicaton describing the model used.