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- W4323857553 abstract "The ability to efficiently isolate antigen-specific B cells in high throughput will greatly accelerate the discovery of therapeutic monoclonal antibodies (mAbs) and catalyze rational vaccine development. Traditional mAb discovery is a costly and labor-intensive process, although recent advances in single-cell genomics using emulsion microfluidics allow simultaneous processing of thousands of individual cells. Here we present a streamlined method for isolation and analysis of large numbers of antigen-specific B cells, including next generation antigen barcoding and an integrated computational framework for B cell multi-omics. We demonstrate the power of this approach by recovering thousands of antigen-specific mAbs, including the efficient isolation of extremely rare precursors of VRC01-class and IOMA-class broadly neutralizing HIV mAbs." @default.
- W4323857553 created "2023-03-11" @default.
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- W4323857553 date "2023-03-10" @default.
- W4323857553 modified "2023-09-27" @default.
- W4323857553 title "Efficient isolation of rare B cells using next-generation antigen barcoding" @default.
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- W4323857553 doi "https://doi.org/10.3389/fcimb.2022.962945" @default.
- W4323857553 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36968243" @default.
- W4323857553 hasPublicationYear "2023" @default.
- W4323857553 type Work @default.