Estimate contrasts using Wald Test
Estimate contrasts using Wald Test
See also
Other modelling:
Contrasts,
ContrastsLimma,
ContrastsMissing,
ContrastsModerated,
ContrastsModeratedDEqMS,
ContrastsPlotter,
ContrastsProDA,
ContrastsROPECA,
ContrastsTable,
INTERNAL_FUNCTIONS_BY_FAMILY,
LR_test(),
Model,
ModelFirth,
ModelLimma,
build_model(),
build_model_limma(),
build_model_logistf(),
contrasts_fisher_exact(),
get_anova_df(),
get_complete_model_fit(),
get_p_values_pbeta(),
group_label(),
isSingular_lm(),
linfct_all_possible_contrasts(),
linfct_factors_contrasts(),
linfct_from_model(),
linfct_matrix_contrasts(),
merge_contrasts_results(),
model_analyse(),
model_summary(),
moderated_p_deqms(),
moderated_p_deqms_long(),
moderated_p_limma(),
moderated_p_limma_long(),
my_contest(),
my_contrast(),
my_contrast_V1(),
my_contrast_V2(),
my_glht(),
pivot_model_contrasts_2_Wide(),
plot_lmer_peptide_predictions(),
sim_build_models_lm(),
sim_build_models_lmer(),
sim_build_models_logistf(),
sim_make_model_lm(),
sim_make_model_lmer(),
strategy_limma(),
strategy_logistf(),
summary_ROPECA_median_p.scaled()
Super class
prolfqua::ContrastsInterface -> ContrastFrith
Public fields
modelsModel
contrastscharacter with contrasts
modelNamename of model
subject_Idname of column containing e.g., protein Id's
p.adjustfunction to adjust p-values (default prolfqua::adjust_p_values)
contrast_resultdata frame containing results of contrast computation
Methods
Inherited methods
Method new()
initialize create Contrast
Usage
ContrastsFirth$new(
model,
contrasts,
p.adjust = prolfqua::adjust_p_values,
modelName = "WaldTestFirth"
)Arguments
modela dataframe with a structure similar to that generated by
build_modelcontrastsa character vector with contrast specificiation
p.adjustfunction to adjust the p-values
modelNamename of contrast method, default WaldTest
Method get_Plotter()
return ContrastsPlotter
creates Contrast_Plotter
Arguments
FCthresholdfold change threshold to show in plots
FDRthresholdFDR threshold to show in plots
Method to_wide()
convert to wide format
Usage
ContrastsFirth$to_wide(columns = c("p.value", "FDR", "statistic"))Examples
modi <- sim_build_models_logistf(model = "parallel3", weight_missing = 1)
#> creating sampleName from fileName column
#> completing cases
#> completing cases done
#> setup done
#> completing cases
#> Joining with `by = join_by(protein_Id)`
#> Joining with `by = join_by(protein_Id)`
contrasts <- c(Avs = "group_A - group_B", AvsCtrl = "group_A - group_Ctrl")
ctr <- ContrastsFirth$new(modi,contrasts)
ctr$get_contrast_sides()
#> # A tibble: 2 × 3
#> contrast group_1 group_2
#> <chr> <chr> <chr>
#> 1 Avs group_A group_B
#> 2 AvsCtrl group_A group_Ctrl
ctr$get_linfct()
#> <ContrastFrith>
#> Inherits from: <ContrastsInterface>
#> Public:
#> clone: function (deep = FALSE)
#> column_description: function ()
#> contrast_result: NULL
#> contrasts: group_A - group_B group_A - group_Ctrl
#> get_Plotter: function (FCthreshold = 1, FDRthreshold = 0.1)
#> get_contrast_sides: function ()
#> get_contrasts: function (all = FALSE)
#> get_linfct: function (avg = TRUE)
#> initialize: function (model, contrasts, p.adjust = prolfqua::adjust_p_values,
#> modelName: WaldTestFirth
#> models: ModelFirth, ModelInterface, R6
#> p.adjust: function (mm, column = "p.value", group_by_col = "contrast",
#> subject_Id: protein_Id
#> to_wide: function (columns = c("p.value", "FDR", "statistic"))
ctr$get_contrasts()
#> determine linear functions:
#> get_contrasts -> contrasts_linfct
#> contrasts_linfct_firth
#> Joining with `by = join_by(protein_Id, contrast)`
#> # A tibble: 20 × 13
#> # Groups: contrast [2]
#> modelName protein_Id contrast sigma df diff FDR std.error statistic
#> <chr> <chr> <chr> <dbl> <int> <dbl> <dbl> <dbl> <dbl>
#> 1 WaldTest… 0EfVhX~00… Avs 1 9 -8.47e- 1 0.769 1.32 -6.40e- 1
#> 2 WaldTest… 0EfVhX~00… AvsCtrl 1 9 -8.47e- 1 0.769 1.32 -6.40e- 1
#> 3 WaldTest… 7cbcrd~57… Avs 1 9 6.90e-16 1 1.38 5.00e-16
#> 4 WaldTest… 7cbcrd~57… AvsCtrl 1 9 8.47e- 1 0.769 1.32 6.40e- 1
#> 5 WaldTest… 9VUkAq~47… Avs 1 9 -8.47e- 1 0.769 1.32 -6.40e- 1
#> 6 WaldTest… 9VUkAq~47… AvsCtrl 1 9 8.47e- 1 0.769 1.32 6.40e- 1
#> 7 WaldTest… BEJI92~52… Avs 1 9 8.47e- 1 0.769 1.32 6.40e- 1
#> 8 WaldTest… BEJI92~52… AvsCtrl 1 9 2.20e+ 0 0.769 1.74 1.26e+ 0
#> 9 WaldTest… CGzoYe~21… Avs 1 9 1.52e-15 1 2.11 7.20e-16
#> 10 WaldTest… CGzoYe~21… AvsCtrl 1 9 1.07e-15 1 2.11 5.08e-16
#> 11 WaldTest… DoWup2~58… Avs 1 9 -1.35e+ 0 0.769 1.78 -7.58e- 1
#> 12 WaldTest… DoWup2~58… AvsCtrl 1 9 -3.04e+ 0 0.769 1.78 -1.71e+ 0
#> 13 WaldTest… Fl4JiV~86… Avs 1 9 8.47e- 1 0.769 1.32 6.40e- 1
#> 14 WaldTest… Fl4JiV~86… AvsCtrl 1 9 8.47e- 1 0.769 1.32 6.40e- 1
#> 15 WaldTest… HvIpHG~90… Avs 1 9 -1.69e+ 0 0.769 1.38 -1.23e+ 0
#> 16 WaldTest… HvIpHG~90… AvsCtrl 1 9 -1.69e+ 0 0.769 1.38 -1.23e+ 0
#> 17 WaldTest… JcKVfU~96… Avs 1 9 1.52e-15 1 2.11 7.20e-16
#> 18 WaldTest… JcKVfU~96… AvsCtrl 1 9 1.07e-15 1 2.11 5.08e-16
#> 19 WaldTest… SGIVBl~57… Avs 1 9 1.35e+ 0 0.769 1.78 7.58e- 1
#> 20 WaldTest… SGIVBl~57… AvsCtrl 1 9 -4.13e-16 1 2.11 -1.96e-16
#> # ℹ 4 more variables: p.value <dbl>, conf.low <dbl>, conf.high <dbl>,
#> # avgAbd <dbl>
mod3 <- sim_build_models_logistf(model = "parallel3", weight_missing = 1, peptide=TRUE)
#> creating sampleName from fileName column
#> completing cases
#> completing cases done
#> setup done
#> completing cases
#> Joining with `by = join_by(protein_Id)`
#> Joining with `by = join_by(protein_Id)`
#> Joining with `by = join_by(protein_Id)`
#> Joining with `by = join_by(protein_Id)`
ctrpep <- ContrastsFirth$new(mod3,contrasts)
ctrpep$get_contrast_sides()
#> # A tibble: 2 × 3
#> contrast group_1 group_2
#> <chr> <chr> <chr>
#> 1 Avs group_A group_B
#> 2 AvsCtrl group_A group_Ctrl
ctrpep$get_linfct()
#> <ContrastFrith>
#> Inherits from: <ContrastsInterface>
#> Public:
#> clone: function (deep = FALSE)
#> column_description: function ()
#> contrast_result: NULL
#> contrasts: group_A - group_B group_A - group_Ctrl
#> get_Plotter: function (FCthreshold = 1, FDRthreshold = 0.1)
#> get_contrast_sides: function ()
#> get_contrasts: function (all = FALSE)
#> get_linfct: function (avg = TRUE)
#> initialize: function (model, contrasts, p.adjust = prolfqua::adjust_p_values,
#> modelName: WaldTestFirth
#> models: ModelFirth, ModelInterface, R6
#> p.adjust: function (mm, column = "p.value", group_by_col = "contrast",
#> subject_Id: protein_Id
#> to_wide: function (columns = c("p.value", "FDR", "statistic"))
ctrpep$get_contrasts()
#> determine linear functions:
#> get_contrasts -> contrasts_linfct
#> contrasts_linfct_firth
#> contrasts_linfct_firth
#> Joining with `by = join_by(protein_Id, contrast)`
#> # A tibble: 20 × 13
#> # Groups: contrast [2]
#> modelName protein_Id contrast sigma df diff FDR std.error statistic
#> <chr> <chr> <chr> <dbl> <int> <dbl> <dbl> <dbl> <dbl>
#> 1 WaldTest… 0EfVhX~00… Avs 1 31 -1.02e+ 0 0.463 0.838 -1.22e+ 0
#> 2 WaldTest… 0EfVhX~00… AvsCtrl 1 31 -6.45e-10 1 0.822 -7.84e-10
#> 3 WaldTest… BEJI92~52… Avs 1 20 1.41e-10 1.000 1.04 1.35e-10
#> 4 WaldTest… BEJI92~52… AvsCtrl 1 20 -2.99e-16 1 1.04 -2.88e-16
#> 5 WaldTest… Fl4JiV~86… Avs 1 42 -7.13e- 1 0.518 0.695 -1.03e+ 0
#> 6 WaldTest… Fl4JiV~86… AvsCtrl 1 42 7.75e- 1 0.485 0.724 1.07e+ 0
#> 7 WaldTest… HvIpHG~90… Avs 1 20 -1.98e+ 0 0.425 1.09 -1.81e+ 0
#> 8 WaldTest… HvIpHG~90… AvsCtrl 1 20 -1.35e+ 0 0.485 0.984 -1.37e+ 0
#> 9 WaldTest… JcKVfU~96… Avs 1 75 -1.24e+ 0 0.463 0.879 -1.41e+ 0
#> 10 WaldTest… JcKVfU~96… AvsCtrl 1 75 -6.86e- 1 0.531 0.763 -8.99e- 1
#> 11 WaldTest… SGIVBl~57… Avs 1 64 -7.95e- 1 0.463 0.630 -1.26e+ 0
#> 12 WaldTest… SGIVBl~57… AvsCtrl 1 64 -7.95e- 1 0.485 0.630 -1.26e+ 0
#> 13 WaldTest… 7cbcrd~57… Avs 1 9 8.47e- 1 0.598 1.32 6.40e- 1
#> 14 WaldTest… 7cbcrd~57… AvsCtrl 1 9 1.69e+ 0 0.485 1.38 1.23e+ 0
#> 15 WaldTest… 9VUkAq~47… Avs 1 9 -1.35e+ 0 0.585 1.78 -7.58e- 1
#> 16 WaldTest… 9VUkAq~47… AvsCtrl 1 9 -4.39e+ 0 0.485 2.11 -2.08e+ 0
#> 17 WaldTest… CGzoYe~21… Avs 1 9 1.35e+ 0 0.585 1.78 7.58e- 1
#> 18 WaldTest… CGzoYe~21… AvsCtrl 1 9 -4.13e-16 1 2.11 -1.96e-16
#> 19 WaldTest… DoWup2~58… Avs 1 9 4.39e+ 0 0.425 2.11 2.08e+ 0
#> 20 WaldTest… DoWup2~58… AvsCtrl 1 9 3.04e+ 0 0.485 1.78 1.71e+ 0
#> # ℹ 4 more variables: p.value <dbl>, conf.low <dbl>, conf.high <dbl>,
#> # avgAbd <dbl>
pl <- ctrpep$get_Plotter()