CASB: a concanavalin A‐based sample barcoding strategy for single‐cell sequencing

Abstract Sample multiplexing facilitates single‐cell sequencing by reducing costs, revealing subtle difference between similar samples, and identifying artifacts such as cell doublets. However, universal and cost‐effective strategies are rather limited. Here, we reported a concanavalin A‐based sampl...

Full description

Bibliographic Details
Main Authors: Liang Fang, Guipeng Li, Zhiyuan Sun, Qionghua Zhu, Huanhuan Cui, Yunfei Li, Jingwen Zhang, Weizheng Liang, Wencheng Wei, Yuhui Hu, Wei Chen
Format: Article
Language:English
Published: Wiley 2021-04-01
Series:Molecular Systems Biology
Subjects:
Online Access:https://doi.org/10.15252/msb.202010060
id doaj-ebc718c2af1444ad82d6c34afa66d132
record_format Article
spelling doaj-ebc718c2af1444ad82d6c34afa66d1322021-08-02T22:11:48ZengWileyMolecular Systems Biology1744-42922021-04-01174n/an/a10.15252/msb.202010060CASB: a concanavalin A‐based sample barcoding strategy for single‐cell sequencingLiang Fang0Guipeng Li1Zhiyuan Sun2Qionghua Zhu3Huanhuan Cui4Yunfei Li5Jingwen Zhang6Weizheng Liang7Wencheng Wei8Yuhui Hu9Wei Chen10Shenzhen Key Laboratory of Gene Regulation and Systems Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaShenzhen Key Laboratory of Gene Regulation and Systems Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaDepartment of Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaShenzhen Key Laboratory of Gene Regulation and Systems Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaShenzhen Key Laboratory of Gene Regulation and Systems Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaDepartment of Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaDepartment of Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaDepartment of Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaDepartment of Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaShenzhen Key Laboratory of Gene Regulation and Systems Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaShenzhen Key Laboratory of Gene Regulation and Systems Biology School of Life Sciences Southern University of Science and Technology Shenzhen ChinaAbstract Sample multiplexing facilitates single‐cell sequencing by reducing costs, revealing subtle difference between similar samples, and identifying artifacts such as cell doublets. However, universal and cost‐effective strategies are rather limited. Here, we reported a concanavalin A‐based sample barcoding strategy (CASB), which could be followed by both single‐cell mRNA and ATAC (assay for transposase‐accessible chromatin) sequencing techniques. The method involves minimal sample processing, thereby preserving intact transcriptomic or epigenomic patterns. We demonstrated its high labeling efficiency, high accuracy in assigning cells/nuclei to samples regardless of cell type and genetic background, and high sensitivity in detecting doublets by three applications: 1) CASB followed by scRNA‐seq to track the transcriptomic dynamics of a cancer cell line perturbed by multiple drugs, which revealed compound‐specific heterogeneous response; 2) CASB together with both snATAC‐seq and scRNA‐seq to illustrate the IFN‐γ‐mediated dynamic changes on epigenome and transcriptome profile, which identified the transcription factor underlying heterogeneous IFN‐γ response; and 3) combinatorial indexing by CASB, which demonstrated its high scalability.https://doi.org/10.15252/msb.202010060CASBcombinatorial sample indexingsample multiplexingsingle‐cell RNA sequencingsingle‐nucleus ATAC sequencing
collection DOAJ
language English
format Article
sources DOAJ
author Liang Fang
Guipeng Li
Zhiyuan Sun
Qionghua Zhu
Huanhuan Cui
Yunfei Li
Jingwen Zhang
Weizheng Liang
Wencheng Wei
Yuhui Hu
Wei Chen
spellingShingle Liang Fang
Guipeng Li
Zhiyuan Sun
Qionghua Zhu
Huanhuan Cui
Yunfei Li
Jingwen Zhang
Weizheng Liang
Wencheng Wei
Yuhui Hu
Wei Chen
CASB: a concanavalin A‐based sample barcoding strategy for single‐cell sequencing
Molecular Systems Biology
CASB
combinatorial sample indexing
sample multiplexing
single‐cell RNA sequencing
single‐nucleus ATAC sequencing
author_facet Liang Fang
Guipeng Li
Zhiyuan Sun
Qionghua Zhu
Huanhuan Cui
Yunfei Li
Jingwen Zhang
Weizheng Liang
Wencheng Wei
Yuhui Hu
Wei Chen
author_sort Liang Fang
title CASB: a concanavalin A‐based sample barcoding strategy for single‐cell sequencing
title_short CASB: a concanavalin A‐based sample barcoding strategy for single‐cell sequencing
title_full CASB: a concanavalin A‐based sample barcoding strategy for single‐cell sequencing
title_fullStr CASB: a concanavalin A‐based sample barcoding strategy for single‐cell sequencing
title_full_unstemmed CASB: a concanavalin A‐based sample barcoding strategy for single‐cell sequencing
title_sort casb: a concanavalin a‐based sample barcoding strategy for single‐cell sequencing
publisher Wiley
series Molecular Systems Biology
issn 1744-4292
publishDate 2021-04-01
description Abstract Sample multiplexing facilitates single‐cell sequencing by reducing costs, revealing subtle difference between similar samples, and identifying artifacts such as cell doublets. However, universal and cost‐effective strategies are rather limited. Here, we reported a concanavalin A‐based sample barcoding strategy (CASB), which could be followed by both single‐cell mRNA and ATAC (assay for transposase‐accessible chromatin) sequencing techniques. The method involves minimal sample processing, thereby preserving intact transcriptomic or epigenomic patterns. We demonstrated its high labeling efficiency, high accuracy in assigning cells/nuclei to samples regardless of cell type and genetic background, and high sensitivity in detecting doublets by three applications: 1) CASB followed by scRNA‐seq to track the transcriptomic dynamics of a cancer cell line perturbed by multiple drugs, which revealed compound‐specific heterogeneous response; 2) CASB together with both snATAC‐seq and scRNA‐seq to illustrate the IFN‐γ‐mediated dynamic changes on epigenome and transcriptome profile, which identified the transcription factor underlying heterogeneous IFN‐γ response; and 3) combinatorial indexing by CASB, which demonstrated its high scalability.
topic CASB
combinatorial sample indexing
sample multiplexing
single‐cell RNA sequencing
single‐nucleus ATAC sequencing
url https://doi.org/10.15252/msb.202010060
work_keys_str_mv AT liangfang casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT guipengli casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT zhiyuansun casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT qionghuazhu casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT huanhuancui casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT yunfeili casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT jingwenzhang casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT weizhengliang casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT wenchengwei casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT yuhuihu casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
AT weichen casbaconcanavalinabasedsamplebarcodingstrategyforsinglecellsequencing
_version_ 1721226460295856128