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10.1016/j.coisb.2020.10.008 http://scihub22266oqcxt.onion/10.1016/j.coisb.2020.10.008 33102951!7568503!33102951     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Curr+Opin+Syst+Biol 2020 ; 24 (ä): 93-99 Nephropedia Template TP {{tp|p=33102951|t=2020. Beyond bulk single-chain sequencing: Getting at the whole receptor |pdf=|usr=}}{{33102951}} gab.com Text Beyond bulk single-chain sequencing: Getting at the whole receptor JO: Curr Opin Syst Biol http://www.kidney.de/pget.php?&tw=1&pmid=33102951 #FOAvip Recent advancements in paired B-cell receptor sequencing technologies have accelerated the development of simpler, high-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 wells and emulsion-based workflows addresses key challenges by improving throughput of single-cell analyses, reducing method complexity, and integrating functional assays into existing workflows. Enabled by paired B-cell receptor sequencing, functional characterization of pathogen-specific antibodies reveals immunological insights beyond bulk sequencing. Twit Text FOAVip Beyond bulk single-chain sequencing: Getting at the whole receptor ????Curr Opin Syst Biol http://www.kidney.de/pget.php?&tw=1&pmid=33102951 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33102951 #FOAvip English Wikipedia <ref>{{Cite pmid|33102951}}</ref> Beyond bulk single-chain sequencing: Getting at the whole receptor #MMPMID33102951 Curtis NC; Lee J Curr Opin Syst Biol 2020[Dec]; 24 (ä): 93-99 PMID33102951show ga Recent advancements in paired B-cell receptor sequencing technologies have accelerated the development of simpler, high-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 wells and emulsion-based workflows addresses key challenges by improving throughput of single-cell analyses, reducing method complexity, and integrating functional assays into existing workflows. Enabled by paired B-cell receptor sequencing, functional characterization of pathogen-specific antibodies reveals immunological insights beyond bulk sequencing. äBeyond bulk single-chain sequencing: Getting at the whole receptor (epmc).pdf DeepDyve Pubget Overpricing