Compound models and Pearson residuals for single-cell RNA-seq data without UMIs

Abstract

Before downstream analysis can reveal biological signals in single-cell RNA sequencing data, normalization and variance stabilization are required to remove technical noise. Recently, Pearson residuals based on negative binomial models have been suggested as an efficient normalization approach. These methods were developed for UMI-based sequencing protocols, where unique molecular identifiers (UMIs) help to remove PCR amplification noise by keeping track of the original molecules. In contrast, full-length protocols such as Smart-seq2 lack UMIs and retain amplification noise, making negative binomial models inapplicable. Here, we extend Pearson residuals to such read count data by modeling them as a compound process: we assume that the captured RNA molecules follow the negative binomial distribution, but are replicated according to an amplification distribution. Based on this model, we introduce compound Pearson residuals and show that they can be analytically obtained without explicit knowledge of the amplification distribution. Further, we demonstrate that compound Pearson residuals lead to a biologically meaningful gene selection and low-dimensional embeddings of complex Smart-seq2 datasets. Finally, we empirically study amplification distributions across several sequencing protocols, and suggest that they can be described by a broken power law. We show that the resulting compound distribution captures overdispersion and zero-inflation patterns characteristic of read count data. In summary, compound Pearson residuals provide an efficient and effective way to normalize read count data based on simple mechanistic assumptions.