Compression of quantification uncertainty for scRNA-seq counts
Scott Van BureniD, Hirak SarkariD, Avi SrivastavaiD, Naim U. RashidiD, Rob PatroiD, Michael I. LoveiD
Abstract
Motivation Quantification estimates of gene expression from single-cell RNA-seq (scRNA-seq) data have inherent uncertainty due to reads that map to multiple genes. Many existing scRNA-seq quantification pipelines ignore multi-mapping reads and therefore underestimate expected read counts for many genes. alevin accounts for multi-mapping reads and allows for the generation of “inferential replicates”, which reflect quantification uncertainty. Previous methods have shown improved performance when incorporating these replicates into statistical analyses, but storage and use of these replicates increases computation time and memory requirements.Results We demonstrate that storing only the mean and variance from a set of inferential replicates (“compression”) is sufficient to capture gene-level quantification uncertainty. Using these values, we generate “pseudo-inferential” replicates from a negative binomial distribution and propose a general procedure for incorporating these replicates into a proposed statistical testing framework. We show reduced false positives when applying this procedure to trajectory-based differential expression analyses. We additionally extend the Swish method to incorporate pseudo-inferential replicates and demonstrate improvements in computation time and memory consumption without any loss in performance. Lastly, we show that the removal of multi-mapping reads can result in significant underestimation of counts for functionally important genes in a real dataset.Availability and implementation makeInfReps and splitSwish are implemented in the development branch of the R/Bioconductor fishpond package available at http://bioconductor.org/packages/devel/bioc/html/fishpond.html. Sample code to calculate the uncertainty-aware p-values can be found on GitHub at https://github.com/skvanburen/scUncertaintyPaperCode.Contact michaelisaiahlove{at}gmail.comCompeting Interest StatementThe authors have declared no competing interest.View Full Text
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 7
- FWCI
- 0.24
- Field percentile
- 41th percentile
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Quantile normalization of single-cell RNA-seq read counts without unique molecular identifiers
F. William Townes, Rafael A. Irizarry·Genome biologyPeer-reviewed·Jul 3, 2020
- Nonparametric expression analysis using inferential replicate counts
Anqi Zhu, Avi Srivastava, … Michael I. Love·Nucleic Acids ResearchPeer-reviewed·Jul 11, 2019
- SAVER: Gene expression recovery for UMI-based single cell RNA sequencing
Mo Chao Huang, Jingshu Wang, … Nancy Ruonan Zhang·Nature MethodsPeer-reviewed·Jun 22, 2018
- Dividing out quantification uncertainty allows efficient assessment of differential transcript expression with edgeR
Pedro L. Baldoni, Yunshun Chen, … Gordon K. Smyth·Nucleic Acids ResearchPeer-reviewed·Nov 21, 2023
- A Bayesian framework for inter-cellular information sharing improves dscRNA-seq quantification
Avi Srivastava, Laraib Iqbal Malik, … Rob Patro·BioinformaticsPeer-reviewed·Jun 23, 2020
- Reliable and accurate gene expression quantification with subpopulation structure-aware constraints for single-cell RNA sequencing
Ching-Chih Tu, Jui‐Hung Hung·bioRxiv·Nov 8, 2022