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.
Authors
- Junjiang He (ORCID: https://orcid.org/0000-0001-7040-2425)
- Hongxia Wang (ORCID: https://orcid.org/0009-0009-3145-4674)
- Ao Liu (ORCID: https://orcid.org/0000-0001-6393-6648)
- Beibei Li (ORCID: https://orcid.org/0000-0002-0485-1975)
- Wenbo Fang
- Wenshan Li (ORCID: https://orcid.org/0000-0003-4434-0712)
Institutions
- Sichuan University (CN)
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
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China