Summary of the NGS data in the unselected and selected libraries.
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a: Number of raw sequences that pass the quality-filtering steps. b: Number of sequences, variants, or peptides mutants that have the expected CDR lengths and accurate in-frame reading. c: Number of sequences, variants, or peptides mutants that perfectly match the CDR diversification strategy and degenerate codon design. d: Number of unique DNA sequences. e: Number of DNA sequences occurring only one time. Summary of the NGS data in the unselected and selected libraries.
创建时间：
2015-06-05
