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The plans should consider data-production rates and data-loss risks when under development

Written informed consent for participation was not required from the participants or the participants legal guardians/next of kin in accordance with the national legislation and institutional requirements

Clinical trials, observational studies, case series, and reports were included

Uniquely mapped reads, aligned with high confidence to a single genomic location, ranged between 2538 million reads per sample

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And again, it comes into, it's not a black or white