Thanks very much for your detailed response!
I am wondering if the Groomer tool is a strictly necessary step after BCL to FASTQ conversion with an Illumina Nextseq500 output, or if it is used for converting sequencing files from less-utilized platforms? I'm building my workflow and don't want to use unnecessary resources.
1 answer
If you are asking in the context of galaxy then perhaps it may only be essential to identify a dataset as sanger fastq format (phred+33) (though I thought one could edit that information directly using the pencil icon and choosing the dataset format as fastqsanger, sorry I have not used galaxy recently).
Edit: This page indicates other functions that fastq groomer may be doing in Galaxy.
Data generated by illumina sequencers for the past 3+ years has been in sanger fastq format and as such does not require "grooming" (outside of galaxy).
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