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Sorry for the delay in answer - I have somehow missed your issue! Every entry in the file list would be considered as a separate sample. So if you have two files for paired-end reads, you would need to concatenate them prior to the analysis, exactly as you said.
I have Illumina short-read sequences I want to use as an input will the tool take that into account when creating a database?
The samples are labeled as
Sample1_R1.fasta Sample1_R2.fasta
would I put that all into the input list file so it reads like:Would the tool recognize short read inputs? Or should I merge the two files so it only takes one input for that particular sample?
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