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10.1016/j.crmeth.2021.100056

http://scihub22266oqcxt.onion/10.1016/j.crmeth.2021.100056
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35475142!9017149!35475142
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suck abstract from ncbi


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pmid35475142      Cell+Rep+Methods 2021 ; 1 (4): 100056
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  • Improved integration of single-cell transcriptome and surface protein expression by LinQ-View #MMPMID35475142
  • Li L; Dugan HL; Stamper CT; Lan LY; Asby NW; Knight M; Stovicek O; Zheng NY; Madariaga ML; 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
  • Cell Rep Methods 2021[Aug]; 1 (4): 100056 PMID35475142show ga
  • 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).
  • |*COVID-19/genetics[MESH]
  • |*Transcriptome/genetics[MESH]
  • |Cluster Analysis[MESH]
  • |Humans[MESH]
  • |Membrane Proteins[MESH]
  • |SARS-CoV-2/genetics[MESH]
  • |Sequence Analysis, RNA/methods[MESH]


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