A Mixture Model Based Read Simulating Method for Single Cell RNA Sequencing

Techniques for single-cell RNA sequencing (scRNA-seq) has enabled unprecedented insights into gene expressions in cell level. Drop-seq is one of the prominent scRNA-seq protocols, and there has been a rapid growth in related analysis tools for Drop-seq data. These methods are tested either using spike-in experiments or on simulation datasets as the real word gene differential expressions are usually unknown. Since spike-in experiments are expensive and time consuming, simulated datasets have become a reasonable alternative method. However, current RNA-seq simulators mostly target at bulk RNA sequencing, which provokes the need of a scRNA-seq simulator for the Drop-seq technology. In this paper, we present a mixture model based read simulating method to simulate the sequencing reads of a Drop-seq experiment. The proposed method is able to simulate large amounts of Drop-seq reads according to the user's experimental setting. Data generated by the proposed model is a reasonable approximation to real Drop-seq data.

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Publication Details

Journal
MOLECULAR SCIENCES AND APPLICATIONS
Published
2025-11-21
DOI
https://doi.org/10.37394/232023.2025.5.13
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

A Mixture Model Based Read Simulating Method for Single Cell RNA Sequencing

Junjiang He, Hongxia Wang, Ao Liu, Beibei Li et al.
MOLECULAR SCIENCES AND APPLICATIONS
Single-cell and spatial transcriptomics
article

A Mixture Model Based Read Simulating Method for Single Cell RNA Sequencing

Junjiang He, Hongxia Wang, Ao Liu, Beibei Li, Wenbo Fang, Wenshan Li
article en

Abstract

Techniques for single-cell RNA sequencing (scRNA-seq) has enabled unprecedented insights into gene expressions in cell level. Drop-seq is one of the prominent scRNA-seq protocols, and there has been a rapid growth in related analysis tools for Drop-seq data. These methods are tested either using spike-in experiments or on simulation datasets as the real word gene differential expressions are usually unknown. Since spike-in experiments are expensive and time consuming, simulated datasets have become a reasonable alternative method. However, current RNA-seq simulators mostly target at bulk RNA sequencing, which provokes the need of a scRNA-seq simulator for the Drop-seq technology. In this paper, we present a mixture model based read simulating method to simulate the sequencing reads of a Drop-seq experiment. The proposed method is able to simulate large amounts of Drop-seq reads according to the user's experimental setting. Data generated by the proposed model is a reasonable approximation to real Drop-seq data.

MOLECULAR SCIENCES AND APPLICATIONSVol. 5
Sichuan University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 68%
Single-cell and spatial transcriptomics
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