eleozzr/scpsm

Propensity Score Matching enables batch effect corrected imputation in single-cell RNA-seq analysis

Multi-batch integration with scPSM

1 Overview

This repository contains the code for the paper Propensity Score Matching enables batch effect corrected imputation in single-cell RNA-seq analysis by Xu et al.

ScPSM (a propensity score matching method for scRNA-seq data) is a statistical tool useful for simultaneously correcting batch effect, imputing dropout and denoising gene expression.

2 Installation

devtools::install_github("eleozzr/scPSM")

The installation should only take a few seconds. The dependencies of the package are listed in the DESCRIPTION file of the package.

3 Usage

We provide two ways to run our methods. For the fist one, the authors can install scPSM package and then use the internal function psm_integrate. For the second one, the authors can run external R script.

3.1 using scPSM package

Start with the vignette online in ./vignettes/README.md.

3.2 using the main function directly

To perform scPSM, first run the help function in file utils.R, then run the script scPSM_main.R. Then the function psm_integrate will be loaded, we can refer to tutorial_pancreas.md for detail running steps.

psm_integrate <- function(batches, markers, hvg, k.self=10, k.mnn=10,
                          correct.all=TRUE, merge.order=1:4){
                          ...
                          }

Arguments

• batches A list of one or more log-normalized-expression matrices where genes correspond to rows and cells correspond to columns. Each matrix should contain the same number of rows, corresponding to the same genes in the same order. Each matrix represents a batch.
• markers A vector specifying which features used as marker genes to compute propensity scores.
• hvg A vector specifying which features used as HVGs for identifying MNN group.
• k.self An integer scalar specifying the number of nearest neighbors in searching KNNs.
• k.mnn An integer scalar specifying the number of nearest neighbors in matching MNN pairs.
• correct.all A logical scalar specifying whether correction should be applied to all genes, even if only a subset is used for the MNN group identification.
• merge.order An integer vector containing the linear merge order of batches.

Value

• Returns a dgCMatrix of integrated data with rows corresponding to the same genes and columns corresponding to the same cells as in the argument batches.

Note: To run the example require the software R >= 4.0.0, batchelor >= 1.4.0, BiocNeighbors >= 1.6.0 and BiocParallel >= 1.22.0.

4 Simulation Data

The code of generating simulation datasets for Fig 2 and Fig S4 is available in simulation_data.md.

5 Real Data

The original data for the toy example is available in the inst/extdata folder

• pancreas_expression_matrix.rds, Load pancreas_expression_matrix.rds from ./inst/extdata/pancreas_expression_matrix.rds for a dgCMatrix with rows corresponding to 34363 genes and columns corresponding to 6321 cells.
• pancreas_metadata.rds, Load pancreas_metadata.rds from ./inst/extdata/pancreas_metadata.rds to get the batch (the "tech" item) and celltype information for all cells .
• HVGs_1000.txt, HVGs_1000.txt can be extracted from adata.var.index[adata.var["highly_variable"] == True].values by implementing the python function sc.pp.highly_variable_genes(adata, n_top_genes=1000, batch_key='tech') by impoting scanpy as sc, or from obj[["RNA"]]@var.features by implementing the R function FindVariableFeatures(obj, nfeatures = 1000) by library(Seurat).

6 Cheatsheet

You can also refer to this cheatsheet to undersand a common workflow

scpsm's Issues

how to select marker genes?

Hi, great software!
Could you mind explaining how to select the markers? Are they the top gene of each clusters?
best