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Data input #1

@Shellfishgene

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@Shellfishgene

Hi,
I don't understand how to prepare data for MicroPheno. Typically 16S raw data comes as two fastq files per sample, R1 and R1. How do these need to be processed? Joined and one fastq/fastq file per sample? Or like the "Ecological environments" example, with one single fasta file and the samples denoted in the fasta headers?

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