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Abstract Many bioinformatics methods seek to reduce reference bias, but no methods exist to comprehensively measure it. analyzes and categorizes instances of reference bias. It works in various scenarios: when the donor’s variants are known and reads are simulated; when donor variants are known and reads are real; and when variants are unknown and reads are real. Using , we observe that more inclusive graph genomes result in fewer biased sites. We find that end-to-end alignment reduces bias at indels relative to local aligners. Finally, we use to characterize how T2T references improve large-scale bias.
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Analyzing shared references across papers
Lin et al. (Fri,) studied this question.
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Genome biology
Johns Hopkins University
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