Methodological report demonstrates accurate clone resolution in barcoded mutagenized libraries, highlighting improved base-calling for long-read sequencing.
Long-read sequencing technologies, an attractive solution for many applications, often suffer from higher error rates. Alignment of multiple reads can improve base-calling accuracy, but some applications, e.g. sequencing mutagenized libraries where multiple distinct clones differ by one or few variants, require the use of barcodes or unique molecular identifiers. Unfortunately, sequencing errors can interfere with correct barcode identification, and a given barcode sequence may be linked to multiple independent clones within a given library.
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Weile et al. (2024) studied this question.
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