hpepLFQ | R Documentation |
No aggregation of data at the same TMT_Set but different LCMS_Injs.
hpepLFQ(
filelist,
basenames,
set_idxes,
injn_idxes,
are_refs,
are_smpls,
dfs = NULL,
df_sps = NULL,
prot_spec_counts = NULL,
use_spec_counts = FALSE,
dat_dir = NULL,
path_ms1 = NULL,
ms1files = NULL,
temp_dir = NULL,
rt_tol = 30,
mbr_ret_tol = 30,
sp_centers_only = FALSE,
imp_refs = FALSE,
group_psm_by = "pep_seq_modz",
group_pep_by = "gene",
lfq_mbr = FALSE,
rt_step = 0.005,
new_na_species = ".other",
max_mbr_fold = 20
)
filelist |
The name of peptide files (TMTset1_LCMSinj1_Peptide_N.txt) with prepending path. |
basenames |
The basenames corresponding to |
set_idxes |
The TMT_Set indexes corresponding to |
injn_idxes |
The LCMS_Injection indexes corresponding to
|
are_refs |
A logical vector corresponding to |
are_smpls |
A logical vector corresponding to |
dfs |
Lists of peptide tables in correspondence to |
df_sps |
A look-up table between peptide sequences and species. |
prot_spec_counts |
A data frame of protein spectrum counts. |
use_spec_counts |
Logical; use spectrum counts instead of intensities or not. |
dat_dir |
The working directory. |
path_ms1 |
The path to MS1 data files. |
ms1files |
The names of MS1 data files. |
temp_dir |
The path to temporary files. |
rt_tol |
Error tolerance in retention times. |
mbr_ret_tol |
The tolerance in MBR retention time in seconds. |
sp_centers_only |
Logical; for a side-effect to return only the values of species centers. |
imp_refs |
Logical; impute missing references or not. |
group_psm_by |
Group PSMs by. |
group_pep_by |
Group peptides by. |
lfq_mbr |
Logical; if TRUE, performs match-between-run (MBR) with Mzion
LFQ data. Also requires |
rt_step |
The step size in binning retention times. |
new_na_species |
A replace value for NA species. |
max_mbr_fold |
Not used. The maximum absolute fold change in MBR. |
Spreads fields of numeric values: sd_log2_R, log2_R, log2_R, I, N_I by TMT sets.
Also works for LFQ as each sample corresponds to a TMT set.
For single SILAC sample, the values of log2Ratios spreads into MULTIPLE columns of heavy, light etc. Despite, log2Ratios remains NA, just like regular single-sample LFQ. The log2Ratios will be later calculated with calcLFQPepNums that are based on intensity values.
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