Error importing sequences with barcode

I'm trying to import many files to forward and reverse sequences, each one in fasta.gz format. I made my manifest file with barcode but when I run the command, it shows me an error (shown in the image below)
How can I solve it?

In that case, you need to indicate the path to the directory, in which both paired reads are located (forward.fastq.gz and reverse.fastq.gz). In your command, path to the file is provided.
More information can be found here.

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