Abstract
Simultaneous high-throughput ATAC and RNA expression with sequencing (SHARE-seq) profiles transcriptomics and chromatin accessibility in the same cells at high throughput. Here, we present a protocol for multimodal profiling of human kidneys with SHARE-seq. We describe steps for processing fixed nuclei for SHARE-seq split-pool barcoding and library preparation. We also detail how to determine the optimal working concentration of Tn5 transposase for transposition and tagmentation. This protocol allows researchers to generate large-scale single-cell multiomics data at low reagent cost. For complete details on the use and execution of this protocol, please refer to Li et al.1
| Original language | English |
|---|---|
| Article number | 103049 |
| Journal | STAR Protocols |
| Volume | 5 |
| Issue number | 3 |
| DOIs | |
| State | Published - Sep 20 2024 |
Keywords
- ChIPseq
- Genomics
- Molecular Biology
- RNA-seq
- Sequencing
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