Description Usage Arguments Value Examples
The parsed data frame from saas::parse_msgf_mzid function contains sometimes multiple entries for a spectrum. (eg. if sequence can be assigned to multiple protein ids). This function takes care of this by default.
1 2 | preprocess(dat, remove_target_decoy_PSM = TRUE,
remove_multiple_proteins_PSM = FALSE, is_subset = NULL)
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dat |
Data frame generated by the saas::parse_msgf_mzid function. |
remove_target_decoy_PSM |
TRUE to remove PSMs that match both a target and decoy sequence. |
remove_multiple_proteins_PSM |
TRUE to remove PSMs that can be assigned to multiple protein ids. |
is_subset |
Location of fasta file with protein_id of the subset of interest in the fasta headers. |
Data frame with the same columns as “dat”. The column protein_id contains all protein_ids that can be assigned to this PSM. Multiple protein_ids are separated by “;”. When “is_subset” is specified, two columns are added:
TRUE if sequence can be assigned to a subset protein id
TRUE if sequence can be assigned to a non subset protein id
Every spectrum haves only 1 row in the data frame.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 | ## Location of the zipped data files
zip_file_path = system.file("extdata", "extdata.zip", package = "saas")
## Unzip and get the (temporary) location of the mzid file with the MS-GF+ search results from a
## competitive target decoy search of the complete pyrococcus proteome against a pyrococcus dataset.
mzid_file_path = unzip(zip_file_path, 'pyrococcus.mzid',exdir = tempdir())
## Read and parse the mzid file
data = parse_msgf_mzid(mzid_file_path)
## Unzip and get the (temporary) location of the file with fasta headers.
## Each fasta header contains a protein_id from the protein subset of interest.
## These protein_ids match the protein_ids in the mzid result file.
fasta_file_path = unzip(zip_file_path, 'transferase_activity_[GO:0016740].fasta', exdir = tempdir())
## Preprocess the data before FDR estimation.
data_prep = preprocess(data, is_subset = fasta_file_path)
## Estimate the FDR in the subset.
data_result = calculate_fdr(data_prep, score_higher = FALSE)
## Check how many PSMs are retained at the 1% FDR threshold.
table(data_result$FDR_stable < .01)
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