User: redgreen

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redgreen10
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Help! I'm using trimmomatic in Galaxy, but it doesn't recognize a part of input dataset.
... I'm using Trimmomatic to trimming paired end reads. When I set "Single-end or paired-end reads?" to Paired-end (two separate input files), it recognizes files only for Input FASTQ file (R2/second of pair). Therefor, I can choose any fastq files for R2/second pair, on the other hand I could not choo ...
rna-seq software error written 12 months ago by redgreen10 • updated 11 months ago by Jennifer Hillman Jackson25k

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