| Literature DB >> 35622335 |
Nidhi Gupta1, Susanna Marquez2, Cinque Soto3, Elaine C Chen4, Magnolia L Bostick1, Ulrik Stervbo5, Andrew Farmer6.
Abstract
During the course of an immune response to a virus such as influenza, B cells undergo activation, clonal expansion, isotype switching, and somatic hypermutation (SHM). Members of an antigen-experienced B-cell clone can have different sequence features including SHM in the immunoglobulin heavy-chain V (IGHV) gene and can use the same IGVH gene in combination with different constant regions or isotypes (e.g., IgM, IgG, IgA). To study these features of expanded clones in an immune response by AIRR-seq, we provide a bulk RNA-based sequencing experimental procedure with unique molecular identifiers (UMIs) and the accompanying bioinformatics analytical workflow.Entities:
Keywords: AIRR; B cells; BCR; Bulk RNA; Bulk RNA sequencing; Heavy and light chain; Immunoglobulin; Repertoire; Sequencing; UMI
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Year: 2022 PMID: 35622335 DOI: 10.1007/978-1-0716-2115-8_19
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745