Metadata-Version: 2.1
Name: scvi-tools
Version: 0.9.0b1
Summary: Deep generative models for end-to-end analysis of single-cell omics data.
Home-page: https://github.com/YosefLab/scvi-tools
License: BSD-3-Clause
Author: Romain Lopez
Author-email: romain_lopez@gmail.com
Requires-Python: >=3.6.2,<4.0
Classifier: Development Status :: 4 - Beta
Classifier: Intended Audience :: Science/Research
Classifier: License :: OSI Approved :: BSD License
Classifier: Natural Language :: English
Classifier: Operating System :: MacOS :: MacOS X
Classifier: Operating System :: Microsoft :: Windows
Classifier: Operating System :: POSIX :: Linux
Classifier: Programming Language :: Python :: 3
Classifier: Programming Language :: Python :: 3.6
Classifier: Programming Language :: Python :: 3.7
Classifier: Programming Language :: Python :: 3.8
Classifier: Programming Language :: Python :: 3.9
Classifier: Topic :: Scientific/Engineering :: Bio-Informatics
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Project-URL: Documentation, https://scvi-tools.org
Description-Content-Type: text/markdown

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[scvi-tools](https://scvi-tools.org/) (single-cell variational inference
tools) is a package for probabilistic modeling of single-cell omics
data, built on top of [PyTorch](https://pytorch.org) and
[Anndata](https://anndata.readthedocs.io/en/latest/).

# Available implementations of single-cell omics models

scvi-tools contains scalable implementations of several models that
facilitate a broad number of tasks across many omics, including:

-   [scVI](https://rdcu.be/bdHYQ) for analysis of single-cell RNA-seq
    data, as well as its improved differential expression
    [framework](https://www.biorxiv.org/content/biorxiv/early/2019/10/04/794289.full.pdf).
-   [scANVI](https://www.biorxiv.org/content/biorxiv/early/2019/01/29/532895.full.pdf)
    for cell annotation of scRNA-seq data using semi-labeled examples.
-   [totalVI](https://www.biorxiv.org/content/10.1101/2020.05.08.083337v1.full.pdf)
    for analysis of CITE-seq data.
-   [gimVI](https://arxiv.org/pdf/1905.02269.pdf) for imputation of
    missing genes in spatial transcriptomics from scRNA-seq data.
-   [AutoZI](https://www.biorxiv.org/content/biorxiv/early/2019/10/10/794875.full.pdf)
    for assessing gene-specific levels of zero-inflation in scRNA-seq
    data.
-   [LDVAE](https://www.biorxiv.org/content/10.1101/737601v1.full.pdf)
    for an interpretable linear factor model version of scVI.
-   [Stereoscope](https://www.nature.com/articles/s42003-020-01247-y)
    for deconvolution of spatial transcriptomics data.
-   peakVI for analysis of ATAC-seq data.
-   [scArches](https://www.biorxiv.org/content/10.1101/2020.07.16.205997v1)
    for transfer learning from one single-cell atlas to a query dataset
    (currently supports scVI, scANVI and TotalVI).

All these implementations have a high-level API that interacts with
[scanpy](http://scanpy.readthedocs.io/), standard save/load functions,
and support GPU acceleration.

# Fast prototyping of novel probabilistic models

scvi-tools contains the building blocks to prototype novel probablistic
models. These building blocks are powered by popular probabilistic and
machine learning frameworks such as [PyTorch
lightning](https://www.pytorchlightning.ai/), and
[Pyro](https://pyro.ai/).

We recommend checking out the [skeleton
repository](https://github.com/YosefLab/scvi-tools-skeleton), as a
starting point for developing new models into scvi-tools.

# Resources

-   Tutorials, API reference, and installation guides are available in
    the [documentation](https://docs.scvi-tools.org/).
-   For discussion of usage, checkout out our
    [forum](https://discourse.scvi-tools.org).
-   Please use the issues here to submit bug reports.
-   If you\'d like to contribute, check out our [development
    guide](https://docs.scvi-tools.org/en/stable/development.html).
-   If you find a model useful for your research, please consider citing
    the corresponding publication (linked above).

