Improved integration of single-cell transcriptome and surface protein expression by LinQ-View.

TitleImproved integration of single-cell transcriptome and surface protein expression by LinQ-View.
Publication TypeJournal Article
Year of Publication2021
AuthorsLi L, Dugan HL, Stamper CT, Lan LYu-Ling, Asby NW, Knight M, Stovicek O, Zheng N-Y, Madariaga MLucia, Shanmugarajah K, Jansen MO, Changrob S, Utset HA, Henry C, Nelson C, Jedrzejczak RP, Fremont DH, Joachimiak A, Krammer F, Huang J, Khan AA, Wilson PC
JournalCell Rep Methods
Volume1
Issue4
Pagination100056
Date Published2021 Aug 23
ISSN2667-2375
KeywordsCluster Analysis, COVID-19, Humans, Membrane Proteins, SARS-CoV-2, Sequence Analysis, RNA, Single-Cell Analysis, Transcriptome
Abstract

Multimodal advances in single-cell sequencing have enabled the simultaneous quantification of cell surface protein expression alongside unbiased transcriptional profiling. Here, we present LinQ-View, a toolkit designed for multimodal single-cell data visualization and analysis. LinQ-View integrates transcriptional and cell surface protein expression profiling data to reveal more accurate cell heterogeneity and proposes a quantitative metric for cluster purity assessment. Through comparison with existing multimodal methods on multiple public CITE-seq datasets, we demonstrate that LinQ-View efficiently generates accurate cell clusters, especially in CITE-seq data with routine numbers of surface protein features, by preventing variations in a single surface protein feature from affecting results. Finally, we utilized this method to integrate single-cell transcriptional and protein expression data from SARS-CoV-2-infected patients, revealing antigen-specific B cell subsets after infection. Our results suggest LinQ-View could be helpful for multimodal analysis and purity assessment of CITE-seq datasets that target specific cell populations (e.g., B cells).

DOI10.1016/j.crmeth.2021.100056
Custom 1

https://www.ncbi.nlm.nih.gov/pubmed/35475142?dopt=Abstract

Alternate JournalCell Rep Methods
PubMed ID35475142
PubMed Central IDPMC9017149
Grant ListHHSN272201400008C / AI / NIAID NIH HHS / United States
U19 AI057266 / AI / NIAID NIH HHS / United States
75N93019C00062 / AO / NIAID NIH HHS / United States
T32 CA009594 / CA / NCI NIH HHS / United States
U19 AI109946 / AI / NIAID NIH HHS / United States
HHSN272201400005C / AI / NIAID NIH HHS / United States
75N93019C00051 / AI / NIAID NIH HHS / United States
HHSN272201700060C / AI / NIAID NIH HHS / United States
U19 AI082724 / AI / NIAID NIH HHS / United States

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