baredSC: Bayesian approach to retrieve expression distribution of single-cell data.

BMC Bioinformatics

Département d'astronomie, Université de Genève, Chemin Pegasi 51, 1290, Versoix, Geneva, Switzerland.

Published: January 2022

AI Article Synopsis

  • The study highlights the increasing use of single-cell RNA sequencing (scRNA-seq) for analyzing gene expression but emphasizes challenges due to data sparsity and technical noise, particularly from sampling.
  • It introduces a new tool called baredSC, which utilizes a Bayesian approach with a Gaussian mixture model to accurately infer the intrinsic gene expression distribution in both one and two dimensions.
  • baredSC has been demonstrated to effectively recover expression distributions, even in sparse data situations, and is validated with real biological datasets, revealing significant correlations between genes like Hoxd13 and Hoxa11.

Article Abstract

Background: The number of studies using single-cell RNA sequencing (scRNA-seq) is constantly growing. This powerful technique provides a sampling of the whole transcriptome of a cell. However, sparsity of the data can be a major hurdle when studying the distribution of the expression of a specific gene or the correlation between the expressions of two genes.

Results: We show that the main technical noise associated with these scRNA-seq experiments is due to the sampling, i.e., Poisson noise. We present a new tool named baredSC, for Bayesian Approach to Retrieve Expression Distribution of Single-Cell data, which infers the intrinsic expression distribution in scRNA-seq data using a Gaussian mixture model. baredSC can be used to obtain the distribution in one dimension for individual genes and in two dimensions for pairs of genes, in particular to estimate the correlation in the two genes' expressions. We apply baredSC to simulated scRNA-seq data and show that the algorithm is able to uncover the expression distribution used to simulate the data, even in multi-modal cases with very sparse data. We also apply baredSC to two real biological data sets. First, we use it to measure the anti-correlation between Hoxd13 and Hoxa11, two genes with known genetic interaction in embryonic limb. Then, we study the expression of Pitx1 in embryonic hindlimb, for which a trimodal distribution has been identified through flow cytometry. While other methods to analyze scRNA-seq are too sensitive to sampling noise, baredSC reveals this trimodal distribution.

Conclusion: baredSC is a powerful tool which aims at retrieving the expression distribution of few genes of interest from scRNA-seq data.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756634PMC
http://dx.doi.org/10.1186/s12859-021-04507-8DOI Listing

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