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Updated: Jun 27, 2025

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Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq
Published on: March 12, 2021
3.6K
Sample multiplexing for retinal single-cell RNA-sequencing.
Biorxiv : the Preprint Server for Biology
|May 7, 2024
Summary
Sample multiplexing enhances single-cell RNA sequencing (scRNA-seq) precision for rare cell populations. This method tags samples with unique barcodes, enabling accurate analysis of cell types and variations across experiments.
Area of Science:
- Genomics
- Molecular Biology
- Neuroscience
Background:
- Characterizing rare cell populations with microfluidic single-cell RNA sequencing (scRNA-seq) is challenging.
- Current enrichment and pooling methods obscure sample origin and phenotypic data, especially in high-variation experiments.
Conclusions:
- Sample multiplexing is a valuable method for increasing the precision of scRNA-seq analysis.
- This technique is particularly useful for studies involving rare cell populations, disease models, and human samples.

