PropertyValue
?:abstract
  • Recent advancements in paired B cell receptor (BCR) sequencing technologies have accelerated the development of simpler, higher-throughput pipelines for generating native antibody heavy and light chain pairs used to elucidate novel antibodies and provide insights into antibody response against pathogenic targets. These technologies involve single-cell isolation, using either single wells or emulsified droplets to maintain physical separation of individual cells, followed by sequencing. The development of novel single well and emulsion-based workflows address key challenges by improving throughput of single-cell analyses, reducing method complexity, and integrating functional assays into existing workflows. Enabled by paired BCR sequencing, functional characterization of pathogen-specific antibodies reveals immunological insights beyond bulk sequencing.
is ?:annotates of
?:creator
?:doi
?:doi
  • 10.1016/j.coisb.2020.10.008
?:journal
  • Curr_Opin_Syst_Biol
?:license
  • no-cc
?:pmc_json_files
  • document_parses/pmc_json/PMC7568503.xml.json
?:pmcid
?:pmid
?:pmid
  • 33102951.0
?:publication_isRelatedTo_Disease
?:source
  • Elsevier; Medline; PMC
?:title
  • Beyond Bulk Single-chain Sequencing – Getting at the Whole Receptor
?:type
?:year
  • 2020-10-17

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