Description Usage Arguments Value Examples
Multi-Matrix Differential Expression Analysis computes Model-Based statistics for each dataset, the sum of individual statistics is the final statistic. The significance is determined via a permutation test which computed the same statistics and sums them after permuting the values across treatment groups. As is outlined in Karpievitch et al. 2018.
1 2 | prot_level_multi_part(mm_list, treat, prot.info, prot_col_name, nperm = 500,
setseed = 12345, dataset_suffix)
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mm_list |
list of matrices for each experiment, length = number of datasets to compare internal dataset dimentions: numpeptides x numsamples for each dataset |
treat |
list of data frames with treatment information to compute the statistic in same order as mm_list |
prot.info |
list of protein and peptide mapping for each matrix in mm_list, in same order as mm_list |
prot_col_name |
column name in prot.info that contains protein identifiers that link all datasets together. Not that Protein IDs will differ across different organizms and cannot be used as the linking identifier. Function match_linker_ids() produces numeric identifyers that link all datasets together |
nperm |
number of permutations, default = 500, this will take a while, test code with fewer permutations |
setseed |
random number generator seed, default = 12345 |
dataset_suffix |
vector of character strings that corresponds to the dataset being analysed. Same length as mm_list. Names will be appended to the columns names that will be generated for each analysed dataset. For example, if analysing mouse and human data this vector may be: c('Mouse', 'Human') |
data frame with the following columns
Column containing the protien IDs used to link proteins across datasets
Average fold change across all datasets
Permutation-based p-valu for the differences between the groups
Multiple testing adjusted p-values
Statistic computed as a a sum of statistics produced for each dataset
all columns passed into the function for the 1st dataset in the list
Fold changes for individual datasets, these values should average to the FC above. As many columns as there are datasets being analyzed.
p-values for individual datasets. As many columns as there are datasets being analyzed.
Multiple testing adjusted p-values for individual datasets. As many columns as there are datasets being analyzed.
Number of peptides presents in each protien for each dataset. As many columns as there are datasets being analyzed.
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 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 | # Load mouse dataset
data(mm_peptides)
head(mm_peptides)
intsCols = 8:13 # different from parameter names as R uses
# outer name spaces if variable is undefined
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$h.c # check the number of bias trends detected
mm_m_ints_norm = eig_norm2(rv=mm_m_ints_eig1)
mm_prot.info = mm_m_ints_norm$normalized[,1:7]
mm_norm_m = mm_m_ints_norm$normalized[,8:13]
imp_mm = MBimpute(mm_norm_m, grps, prot.info=mm_prot.info,
pr_ppos=2, my.pi=0.05,
compute_pi=FALSE, sseed=131)
# Load human dataset
data(hs_peptides)
head(hs_peptides)
intsCols = 8:13 # different from parameter names as R uses
# outer name spaces if variable is undefined
metaCols = 1:7 # reusing this variable
m_logInts = make_intencities(hs_peptides, intsCols) # will reuse the name
m_prot.info = make_meta(hs_peptides, metaCols)
m_logInts = convert_log2(m_logInts)
grps = as.factor(c('CG','CG','CG', 'mCG','mCG','mCG'))
hs_m_ints_eig1 = eig_norm1(m=m_logInts,treatment=grps,prot.info=m_prot.info)
hs_m_ints_eig1$h.c # check the number of bias trends detected
hs_m_ints_norm = eig_norm2(rv=hs_m_ints_eig1)
hs_prot.info = hs_m_ints_norm$normalized[,1:7]
hs_norm_m = hs_m_ints_norm$normalized[,8:13]
imp_hs = MBimpute(hs_norm_m, grps, prot.info=hs_prot.info,
pr_ppos=2, my.pi=0.05,
compute_pi=FALSE, sseed=131)
# Multi-Matrix Model-based differential expression analysis
# Set up needed variables
mms = list()
treats = list()
protinfos = list()
mms[[1]] = imp_mm$y_imputed
mms[[2]] = imp_hs$y_imputed
treats[[1]] = grps
treats[[2]] = grps
protinfos[[1]] = imp_mm$imp_prot.info
protinfos[[2]] = imp_hs$imp_prot.info
nperm = 50
comb_MBDE = prot_level_multi_part(mm_list=mms, treat=treats,
prot.info=protinfos,
prot_col_name='ProtID', nperm=nperm,
setseed=123, dataset_suffix=c('MM', 'HS'))
# Analysis for proteins only present in mouse,
# there are no proteins suitable for
# Model-Based analysis in human dataset
subset_data = subset_proteins(mm_list=mms, prot.info=protinfos, 'MatchedID')
mm_dd_only = subset_data$sub_unique_mm_list[[1]]
hs_dd_only = subset_data$sub_unique_mm_list[[2]]
protinfos_mm_dd = subset_data$sub_unique_prot.info[[1]]
DE_mCG_CG_mm_dd = peptideLevel_DE(mm_dd_only, grps,
prot.info=protinfos_mm_dd, pr_ppos=2)
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