I used the "Barcode Splitter" tool to split multiplexed RNA-Seq libraries
into separate files. I would now like to map the reads from each of these
fastq files to a reference genome. However, the fastq files generated by
Barcode Splitter don't appear in the "Fastq File" pull-down menus within the
the BWA or Bowtie launch pages. I'm probably missing something obvious, but
what is the trick for making these files available for the mapping tools? Do
I need to import them into my history somehow?

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