Then we need to import a FASTQ pair (e.g. You may rename the name by directly editing it. Click “History Option "icon on the top of History section.All files are available on Zenodo First we need create a new history for this RNA-seq exercise.
#Galaxy sequence analysis archive#
We have extracted sequences from the Sequence Read Archive (SRA) files to build FASTQ files. Moreover, two of the treated and two of the untreated samples are from a paired-end sequencing assay, while the remaining samples are from a single-end sequencing experiment.
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