Description Usage Arguments Value Examples
Function get_presAbs_prots() produces a subset of protein meta data and intencities for multiple datasets pass in as a list. If a single dataset is passed in (list of length one) it will be processed in the same way as longer lists.
1 | get_presAbs_prots(mm_list, prot.info, protnames_norm, prot_col_name)
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mm_list |
list of matrices of intensities for each experiment. Dimentions: numpeptides x numsamples different for each dataset. |
prot.info |
list of protein and peptide metadata/mappings for each matrix in mm_list, data.frames "parallel" to matrices in mm_list. |
protnames_norm |
list of protein pdentifies to be used to determine peptides that will be placed into Presence/Absence analysis category due to too many missing peptides. Taken from the return value from eig_norm2(). |
prot_col_name |
column name (string) that will be used to get ProteinIDs in the raw data matrices |
list of lists of length 2
list of intecities in the same order and of the same length as the number of datasets that were passed into the function
list of protein metadata in the same order and of the same length as the number of datasets that as were passed into the function
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 | #' # Load mouse dataset
data(mm_peptides)
head(mm_peptides)
intsCols = 8:13
metaCols = 1:7 # reusing this variable
m_logInts = make_intencities(mm_peptides, intsCols) # will reuse the name
m_prot.info = make_meta(mm_peptides, metaCols)
m_logInts = convert_log2(m_logInts)
grps = as.factor(c('CG','CG','CG', 'mCG','mCG','mCG'))
mm_m_ints_eig1 = eig_norm1(m=m_logInts,treatment=grps,prot.info=m_prot.info)
mm_m_ints_eig1$h.c # check the number of bias trends detected
mm_m_ints_norm = eig_norm2(rv=mm_m_ints_eig1)
# Load human dataset
data(hs_peptides)
head(hs_peptides)
intsCols = 8:13
metaCols = 1:7 # reusing this variable
m_logInts = make_intencities(hs_peptides, intsCols) # will reuse the name
m_prot.info = make_meta(hs_peptides, metaCols)
m_logInts = convert_log2(m_logInts)
grps = as.factor(c('CG','CG','CG', 'mCG','mCG','mCG'))
hs_m_ints_eig1 = eig_norm1(m=m_logInts,treatment=grps,prot.info=m_prot.info)
hs_m_ints_eig1$h.c # check the number of bias trends detected
hs_m_ints_norm = eig_norm2(rv=hs_m_ints_eig1)
# Set up for presence/absence analysis
raw_list = list()
norm_imp_prot.info_list = list()
raw_list[[1]] = mm_m_ints_eig1$m
raw_list[[2]] = hs_m_ints_eig1$m
norm_imp_prot.info_list[[1]] = mm_m_ints_eig1$prot.info
norm_imp_prot.info_list[[2]] = hs_m_ints_eig1$prot.info
protnames_norm_list = list()
protnames_norm_list[[1]] = unique(mm_m_ints_norm$normalized$MatchedID)
protnames_norm_list[[2]] = unique(hs_m_ints_norm$normalized$MatchedID)
presAbs_dd = get_presAbs_prots(mm_list=raw_list,
prot.info=norm_imp_prot.info_list,
protnames_norm=protnames_norm_list,
prot_col_name=2)
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