snRNA-seq libraries were prepared using the DNBelab C Series Single-Cell Library Prep Set64 (MGI, 1000021082). In brief, single-nucleus suspensions were converted to barcoded snRNA-seq libraries through the generation of droplet, breakage of emulsion, collection of bead, reverse transcription and cDNA amplification. Indexed libraries were performed based on the manufacturer’s protocol. The Qubit ssDNA Assay Kit (Thermo Fisher Scientific, {"type":"entrez-protein","attrs":{"text":"Q10212","term_id":"1723280","term_text":"Q10212"}}Q10212) was used to measure the concentration. Then, the prepared libraries were sequenced using the DNBSEQ-T1 or DNBSEQ-T7 sequencer at the China National GeneBank (Shenzhen, China) and the sequencing strategy was below: 41-bp read as read 1 and 100-bp read as read 2.
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