The interesting thing about this set up is that it outputs a set of un-filtered merged_peptides.fasta and a un-filtered variant_peptides_summary.txt, which I don't think is necessary since merged_peptides filtering should be on. The variant_peptides_summary.txt serves as a sanity check (?) with the fasta entry, but is still unnecessary since the original run that produced the fasta would have given the exact same summary table.
See here for a sample with expression table available. The decoy, encode and split folders all look clean.
Since this sample doesn't have expression table I have to assume that everything in decoy, encode and split are NOT filtered. Which is kind of misleading since the files in those folders are not labelled as "filtered" or "unfiltered". I think for this sample nothing should be outputted?
I am doing
merge_variant_noncoding = 'both'
andfasta
entry withThe interesting thing about this set up is that it outputs a set of un-filtered
merged_peptides.fasta
and a un-filteredvariant_peptides_summary.txt
, which I don't think is necessary sincemerged_peptides
filtering should be on. Thevariant_peptides_summary.txt
serves as a sanity check (?) with the fasta entry, but is still unnecessary since the original run that produced the fasta would have given the exact same summary table.See here for a sample with expression table available. The decoy, encode and split folders all look clean.
But there's a problem with the expression table is NOT available, resulting in:
Since this sample doesn't have expression table I have to assume that everything in decoy, encode and split are NOT filtered. Which is kind of misleading since the files in those folders are not labelled as "filtered" or "unfiltered". I think for this sample nothing should be outputted?