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k-NN-based mapping of cells across representations

Project description

CellMapper

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k-NN-based mapping of cells across representations to tranfer labels, embeddings and expression values. Works for millions of cells, on CPU and GPU, across molecular modalities, between spatial and non-spatial data, for arbitrary query and reference datasets. Using faiss to compute k-NN graphs, CellMapper takes about 30 seconds to transfer cell type labels from 1.5M cells to 1.5M cells on a single RTX 4090 with 60 GB CPU memory.

Inspired by scanpy's ingest and the HNOCA-tools packages. Check out the docs to learn more, in particular our tutorials.

Key use cases

  • Transfer cell type labels and expression values from dissociated to spatial datasets.
  • Transfer embeddings between arbitrary query and reference datasets.
  • Compute presence scores for query datasets in large reference atlasses.
  • Identify niches in spatial datasets by contextualizing latent spaces in spatial coordinates.
  • Evaluate the results of transferring labels, embeddings and feature spaces using a variety of metrics.

The core idea of CellMapper is to separate the method (k-NN graph with some kernel applied to get a mapping matrix) from the application (mapping across arbitrary representations), to be flexible and fast. The tool currently supports pynndescent, sklearn, faiss and rapids for neighborhood search, implements a variety of graph kernels, and is closely integrated with AnnData objects.

Installation

You need to have Python 3.10 or newer installed on your system. If you don't have Python installed, we recommend installing uv.

There are two alternative options to install cellmapper:

  • Install the latest release from PyPI:

    pip install cellmapper
    
  • Install the latest development version:

    pip install git+https://github.com/quadbio/cellmapper.git@main
    

Getting started

This package assumes that you have query and reference AnnData objects, with a joint embedding computed and stored in .obsm. We explicilty do not compute this joint embedding, but there are plenty of method you can use to get such joint embeddings, e.g. GimVI or ENVI for spatial mapping, GLUE, MIDAS and MOFA+ for modality translation, and scVI, scANVI and scArches for query-to-reference mapping - this is just a small selection!

With a joint embedding in .obsm["X_joint"] at hand, the simplest way to use CellMapper is as follows:

from cellmapper import CellMapper

cmap = CellMapper(query, reference).fit(
    use_rep="X_joint", obs_keys="celltype", obsm_keys="X_umap", layer_key="X"
    )

This will transfer data from the reference to the query dataset, including celltype labels stored in reference.obs, a UMAP embedding stored in reference.obsm, and expression values stored in reference.X.

There are many ways to customize this, e.g. use different ways to compute k-NN graphs and to turn them into mapping matrices, and we implement a few methods to evaluate whether your k-NN transfer was sucessful. The tool also implements a self-mapping mode (only a query object, no reference), which is useful for spatial contextualization. Check out the docs to learn more.

Release notes

See the changelog.

Contact

If you found a bug, please use the issue tracker.

Citation

Please cite this GitHub repo if you find CellMapper useful for your research.

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