snRNA-seq library preparation

DW Di-Xian Wang
ZD Zhao-Jun Dong
SD Sui-Xin Deng
YT Ying-Ming Tian
YX Yu-Jie Xiao
XL Xinran Li
XM Xiao-Ru Ma
LL Liang Li
PL Pengxiao Li
HC Hui-Zhong Chang
LL Longqi Liu
FW Fan Wang
YW Yang Wu
XG Xiang Gao
SZ Shuang-Shuang Zheng
HG Hui-Min Gu
YZ Ya-Nan Zhang
JW Jian-Bin Wu
FW Fan Wu
YP Yonglin Peng
XZ Xiao-Wen Zhang
RZ Ren-Ya Zhan
LG Li-Xia Gao
QS Qiming Sun
XG Xing Guo
XZ Xiao-Dong Zhao
JL Jian-Hong Luo
RZ Ruhong Zhou
LH Lei Han
YS Yousheng Shu
JZ Jing-Wei Zhao
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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, 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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