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Shapiro, M

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Traditionally, repertoire screening has been constrained by low-throughput methods that capture a small fraction of the BCRs found in vivo 5,6 , or by high-throughput sequencing strategies which decouple and recombine antibody chains, losing essential pairing optimizations occurring within the B cell germinal center 7,8

10.1016/j.tins.2024.04.003 41 ZoltanU.StefanoT.TamasK.WrenJ

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