Metadata-Version: 2.1
Name: quipcell
Version: 0.8
Summary: Fine-scale cellular deconvolution based on Generalized Cross Entropy
Home-page: https://github.com/genentech/quipcell
Author: Jack Kamm
Author-email: jackkamm@gmail.com
License: MIT
Project-URL: Source, https://github.com/genentech/quipcell/
Platform: any
Classifier: Development Status :: 4 - Beta
Classifier: Programming Language :: Python
Description-Content-Type: text/markdown; charset=UTF-8; variant=GFM
License-File: LICENSE.txt
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Requires-Dist: numpy
Requires-Dist: scipy
Requires-Dist: pandas
Requires-Dist: scikit-learn
Requires-Dist: cvxpy
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Requires-Dist: jaxlib
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Requires-Dist: setuptools; extra == "testing"
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# quipcell

> Fine-scale cellular deconvolution based on Generalized Cross Entropy

A method to perform cellular deconvolution at a fine-scale
(i.e. single-cell or neighborhood level), using a generalization of
maximum entropy that is also an efficient convex optimization problem.

## Installation

Installation

```
pip install quipcell
```

## Method

A preprint describing the method is available on [bioRxiv](https://www.biorxiv.org/content/10.1101/2024.06.07.598010v1).

## Usage

The [documentation](https://genentech.github.io/quipcell/) includes a
[vignette](https://genentech.github.io/quipcell/vignette.html) and
[API reference](https://genentech.github.io/quipcell/api/modules.html).

The snippet below demonstrates how to obtain weights from two
AnnData's containing the single cell reference and the bulk samples to
deconvolve. Both AnnDatas are assumed to contain the raw counts, and
to have the same genes. Dimensionality reduction steps (PCA and LDA)
are run on the single cell reference, then applied to the bulk data,
and then quipcell estimates single cell weights using a generalized
maximum entropy method. The resulting weights represent the
probability that a random read from the bulk sample originated from
"near" the reference cell.

```
import scanpy as sc
from sklearn.discriminant_analysis import LinearDiscriminantAnalysis

# save the number of UMIs per cell
adata_ref.obs['n_umi'] = adata_ref.X.sum(axis=1)

# Normalize the single cell reference
normalize_sum = 1e3
sc.pp.normalize_total(adata_ref, target_sum=normalize_sum)

# Compute low dimensional features via PCA and LDA on the single cells
sc.pp.pca(adata_ref, n_comps=100)

lda = LinearDiscriminantAnalysis(n_components=15)
lda.fit(adata_ref.obsm['X_pca'], adata_ref.obs['celltype'])

adata_ref.obsm['X_lda'] = lda.transform(adata_ref.obsm['X_pca'])

# Normalize the bulk samples
sc.pp.normalize_total(adata_bulk, target_sum=normalize_sum)

# Apply PCA rotation to pseudobulks. Note the centers need to be
# subtracted before rotation
X = adata_bulk.X - np.squeeze(np.asarray(adata_ref.X.mean(axis=0)))
X = np.asarray(X @ adata_ref.varm['PCs'])
adata_bulk.obsm['X_pca'] = X
# Apply LDA rotation to pseudobulks
adata_bulk.obsm['X_lda'] = lda.transform(X)

# Compute the weights. Rows are reference single cells, columns are
# bulk samples. The entries represent the probability that a random
# read from the bulk sample originated near the respective reference
# cell.
w_reads = qpc.estimate_weights_multisample(adata_ref.obsm['X_lda'],
                                         adata_bulk.obsm['X_lda'])
```

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## Note

This project has been set up using PyScaffold 4.5. For details and usage
information on PyScaffold see https://pyscaffold.org/.
