Probabilistic Count Matrix Factorization for Single Cell Expression Data Analysis

PhD
ABS4NGS
MACARON
Statistics
single-cell
conference
RECOMB
Research in Computational Molecular Biology, 22nd Annual International Conference RECOMB 2018, Pierre et Marie Curie Campus, Sorbonne University, Paris (France)
Authors

Ghislain Durif

Laurent Modolo

Jeff E. Mold

Sophie Lambert-Lacroix

Franck Picard

Published

April 23, 2018

Keywords: Statistics, Dimension reduction, Matrix Factorization, Data visualization, Single-cell, Gene expression, RNA-seq

Summary

The development of high throughput single-cell sequencing technologies now allows the investigation of the population level diversity of cellular transcriptomes. This diversity has shown two faces. First, the expression dynamics (gene to gene variability) can be quantified more accurately, thanks to the measurement of lowly-expressed genes. Second, the cell-to-cell variability is high, with a low proportion of cells expressing the same gene at the same time/level. Those emerging patterns appear to be very challenging from the statistical point of view, especially to represent and to provide a summarized view of single-cell expression data. PCA is one of the most powerful framework to provide a suitable representation of high dimensional datasets, by searching for latent directions catching the most variability in the data. Unfortunately, classical PCA is based on Euclidean distances and projections that work poorly in presence of over-dispersed counts that show drop-out events (zero-inflation) like single-cell expression data We propose a probabilistic Count Matrix Factorization (pCMF) approach for single-cell expression data analysis, that relies on a sparse Gamma-Poisson factor model. This hierarchical model is inferred using a variational EM algorithm. It is able to jointly build a low dimensional representation of cells and genes. We show how this probabilistic framework induces a geometry that is suitable for single-cell data visualization, and produces a compression of the data that is very powerful for clustering purposes. Our method is competed against other standard representation methods like t-SNE, and we illustrate its performance for the representation of single-cell data. We especially focus on publicly available single-cell RNA-seq datasets.