Hello fellow Galaxy users,
I am trying to use Trinity to assemble NGS reads from 9 samples that each have paired-end reads. However, I am unable to load multiple Left and Right reads so that all 18 of the fastq files can be run together. I see that input can be of 3 types: single dataset, multiple datasets (batch), and dataset collection. I think what I would want to be using is dataset collection to input the 8 Left and 8 Right reads. My problem is that I have "no dataset collection available", despite uploading the fastq files through the collection tab in the upload window (collection type: list). Any experience with this?
Here is a visual of my problem: