Example Novel Peptide Filter Workflow

Galaxy Workflow ' Example Novel Peptide Filter'


StepAnnotation
Step 1: Input dataset
select at runtime
Step 2: Input dataset
select at runtime
Step 3: Input dataset
select at runtime
Any MS search software may be used to generate this table-formatted (e.g. excel) list of peptide identifications as long as peptide IDs are listed under one column.
Step 4: Concatenate datasets
Output dataset 'output' from step 1
Datasets
Dataset 1
Output dataset 'output' from step 2
Concatenates the reference proteome (Ensembl pep.all) and the contaminants database (cRAP).
Step 5: FASTA-to-Tabular
Output dataset 'out_file1' from step 4
1
0
Convert Reference+cRAP fasta into tabular format. Column 1: Accession Column 2: aa sequence
Step 6: find in reference
Output dataset 'output' from step 3
Output dataset 'output' from step 5
Choose the column of input and reference to compare
2 (value not yet validated)
2 (value not yet validated)
True
lines with no match in reference
No
Input is the list of peptides identified from MS search software. Peptides should be in table format and listed within a column.
Step 7: find in reference
Output dataset 'novel' from step 6
select at runtime
Choose the column of input and reference to compare
2 (value not yet validated)
2 (value not yet validated)
True
lines with match in reference
Yes
1 (value not yet validated)
;
,
Input are list of novel peptides (not present in the reference database) and this step finds to which variations each novel peptide corresponds.