delve-fs 0.1.4

Feature selection for preserving biological trajectories from single-cell data

DELVE

Dynamic selection of locally covarying features

Introduction

DELVE is an unsupervised feature selection method for identifying a representative subset of dynamically-expressed molecular features that recapitulate cellular trajectories from single-cell data (e.g. single-cell RNA sequencing, protein iterative immunofluorescence imaging). In contrast to previous work, DELVE uses a bottom-up approach to mitigate the effect of unwanted sources of feature variation confounding inference, and instead models cell states from dynamic feature modules that constitute core regulatory complexes. For more details on the method, please read the associated preprint: Ranek JS, Stallaert W, Milner J, Stanley N, and Purvis JE. Feature selection for preserving biological trajectories in single-cell data. bioRxiv. 2023.

For a comparison of alternative feature selection methods and the overall benchmarking pipeline, please see delve_benchmark.

Installation

Dependencies

• Python >= 3.6, sketchKH == 0.1.1, anndata >= 0.7.6, numpy >= 1.19.5, scipy >= 1.7.1, pandas >= 1.1.5, umap-learn == 0.5.1, scikit-learn >= 0.23.2, tqdm

You can install the package and necessary dependencies with pip by,

pip install delve-fs

Alternatively, you can clone the git repository and install the necessary dependencies using the provided yml file. First clone the repository by,

git clone https://github.com/jranek/delve.git

Then change the working directory as,

cd delve

You can then create the conda environment using the provided yml file.

conda env create -f venv_delve.yml

Once the environment is created, you can activate it by,

conda activate venv_delve

Data access

You can download all of the preprocessed single-cell datasets (.h5ad files) from the Zenodo repository.

Example usage

To perform trajectory-preserving feature selection with DELVE, first read in a preprocessed .h5ad object. This .h5ad object contains a sample profiled with a single-cell technology (i.e. protein iterative indirect immunofluorescence imaging data).

import anndata
import os
adata = anndata.read_h5ad(os.path.join('data', 'adata_RPE.h5ad'))

Then simply perform DELVE feature selection by,

# Inputs:
# adata: annotated data object (dimensions = cells x features)
# k: number of nearest neighbors in the between-cell kNN affinity graph
# n_pcs: number of principal components. If None (default): will construct a between-cell affinity graph by computing pairwise Euclidean distances according to adata.X. Else: according to PCA of adata.X 
# num_subsamples: number of representative cellular neighborhoods. Neighborhoods are subsampled using kernel herding sketching (see https://dl.acm.org/doi/abs/10.1145/3535508.3545539, https://github.com/CompCy-lab/SketchKH)  
# n_clusters: number of feature modules
# n_random_state: number of random KMeans clustering initializations when identifying dynamic feature modules
# random_state: random state parameter 
# n_jobs: number of tasks
# -----------------------
    
# Returns:
# delta_mean: average pairwise change in expression across prototypical cellular neighborhoods (dimensions = num_subsamples x features)
# modules: dataframe containing feature-cluster assignments and permutation p-values (dimensions = features x 2)
# ranked_features: ranked set of features that best preserve the local trajectory structure (dimensions = features x 1)
# -----------------------
from delve import *
delta_mean, modules, ranked_features = delve_fs(adata = adata, k = 10, num_subsamples = 1000, n_clusters = 5, random_state = 0, n_jobs = -1)

License

This software is licensed under the MIT license (https://opensource.org/licenses/MIT).