A realistic FastQ-based framework FastQDesign for ScRNA-seq study design issues
Single-cell RNA sequencing (scRNA-seq) has emerged as a powerful technology for characterizing transcriptomic profiles at single-cell resolution. It is crucial to consider both the number of cells and sequencing depth during library preparation. The existing methods are primarily simulation-based, rely on Unique Molecular Identifier (UMI) matrix, and have little context in the actual FastQ reads. Here we propose the first FastQ-based study design framework, named "FastQDesign," which leverages raw FastQ files from publicly available datasets as references and suggests an optimal design within a fixed budget. We demonstrate our framework through a synthetic dataset and applications to nine real-world datasets. Our study underscores the importance of an appropriate design to investigate the biology of heterogeneous cell populations and offers practical guidance considering cost-benefit trade-offs. A high-efficiency software suite is available at https://github.com/yuw444/FastQDesign .
Authors
- Kwang Woo Ahn (ORCID: https://orcid.org/0000-0003-4567-8037)
- Yi-Guang Chen (ORCID: https://orcid.org/0000-0001-9616-8841)
- Yu Wang (ORCID: https://orcid.org/0000-0002-4586-5679)
- Chien‐Wei Lin (ORCID: https://orcid.org/0000-0003-4023-7339)
Institutions
- Medical College of Wisconsin (US)
Publication Details
- Journal
- Communications Biology
- Published
- 2025-04-02
- DOI
- https://doi.org/10.1038/s42003-025-07938-8
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Institutes of Health
- National Center for Advancing Translational Sciences