Abstract

Single-cell RNA-sequencing (scRNA-Seq) is a compelling approach to directly and simultaneously measure cellular composition and state, which can otherwise only be estimated by applying deconvolution methods to bulk RNA-Seq estimates. However, it has not yet become a widely used tool in population-scale analyses, due to its prohibitively high cost. Here we show that given the same budget, the statistical power of cell-type-specific expression quantitative trait loci (eQTL) mapping can be increased through low-coverage per-cell sequencing of more samples rather than high-coverage sequencing of fewer samples. We use simulations starting from one of the largest available real single-cell RNA-Seq data from 120 individuals to also show that multiple experimental designs with different numbers of samples, cells per sample and reads per cell could have similar statistical power, and choosing an appropriate design can yield large cost savings especially when multiplexed workflows are considered. Finally, we provide a practical approach on selecting cost-effective designs for maximizing cell-type-specific eQTL power which is available in the form of a web tool.

Highlights

  • Single-cell RNA-sequencing is a compelling approach to directly and simultaneously measure cellular composition and state, which can otherwise only be estimated by applying deconvolution methods to bulk RNA-Seq estimates

  • Ct-expression quantitative trait loci (eQTL) mapping critically depends on assaying many individuals, which is needed in order to achieve sufficient statistical power for detecting true associations

  • In cell-type-specific eQTL studies (ct-eQTL) studies, accurate cell-type-specific expression estimates can be achieved with low-coverage sequencing by pooling cells of the same type

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Summary

Introduction

Single-cell RNA-sequencing (scRNA-Seq) is a compelling approach to directly and simultaneously measure cellular composition and state, which can otherwise only be estimated by applying deconvolution methods to bulk RNA-Seq estimates. It has not yet become a widely used tool in population-scale analyses, due to its prohibitively high cost. The ability to simultaneously estimate cellular composition and state using scRNA-Seq creates an enormous opportunity to apply scRNA-Seq to large population cohorts to detect subtle shifts in single-cell transcriptomics associated with population level variation (e.g., genetics and/or disease status). Despite the recent considerable drop in sequencing cost[23], the total expense of a large-sample single-cell study can still be prohibitively high[24]

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