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Limpa contrast analysis facade

Limpa contrast analysis facade

Value

An R6 class generator.

Details

Encapsulates the pipeline: strategy_limpa -> build_model_limpa -> ContrastsLimma.

Operates as a "same"-level facade: it consumes whatever aggregated LFQData prolfqua's normal aggregation pipeline produced and fits limpa at that hierarchy level. If config$opt_se is set (e.g. when the input came from AggregateLimpa), the per-observation standard error is used as a vooma precision-weight predictor; otherwise plain vooma is fit. The config$nr_children column is required and is used to flag imputed observations (nr_children == 0) for vooma's imputation-aware DF correction.

For nested (peptide/precursor) input that should be rolled up to proteins via limpa's DPC quantification, use ContrastsLimpaNestedFacade instead — that facade owns the AggregateLimpa pre-step.

See also

Other modelling: AnovaExtractor, Contrasts, ContrastsDEqMSFacade, ContrastsDEqMSVoomFacade, ContrastsFirth, ContrastsFirthFacade, ContrastsFirthNestedFacade, ContrastsLMFacade, ContrastsLMImputeFacade, ContrastsLMMissingFacade, ContrastsLimma, ContrastsLimmaFacade, ContrastsLimmaImputeFacade, ContrastsLimmaVoomFacade, ContrastsLimmaVoomImputeFacade, ContrastsLimpaNestedFacade, ContrastsLmerNestedFacade, ContrastsMissing, ContrastsModerated, ContrastsModeratedDEqMS, ContrastsPlotter, ContrastsRLMFacade, ContrastsROPECA, ContrastsROPECANestedFacade, ContrastsRfitFacade, ContrastsTable, INTERNAL_FUNCTIONS_BY_FAMILY, LR_test(), Model, ModelFirth, ModelLimma, StrategyLM, StrategyLimma, StrategyLimpa, StrategyLmer, StrategyLogistf, StrategyRLM, StrategyRfit, build_contrast_analysis(), build_model(), build_model_glm_peptide(), build_model_glm_protein(), build_model_impute(), build_model_limma(), build_model_limma_impute(), build_model_limma_voom(), build_model_limma_voom_impute(), build_model_limpa(), build_model_logistf(), compute_borrowed_variance(), compute_borrowed_variance_limma(), compute_contrast(), compute_lmer_contrast(), contrasts_fisher_exact(), df.residual.rfit_prolfqua(), get_anova_df(), get_complete_model_fit(), get_p_values_pbeta(), group_label(), impute_refit_singular(), is_singular_lm(), linfct_all_possible_contrasts(), linfct_factors_contrasts(), linfct_from_model(), linfct_matrix_contrasts(), list_facades(), lookup_facade(), merge_contrasts_results(), model_analyse(), model_summary(), moderated_p_deqms(), moderated_p_deqms_long(), moderated_p_limma(), moderated_p_limma_long(), new_lm_imputed(), pivot_model_contrasts_to_wide(), plot_lmer_peptide_predictions(), register_facade(), sigma.rfit_prolfqua(), sim_build_models_lm(), sim_build_models_lmer(), sim_build_models_logistf(), sim_make_model_lm(), sim_make_model_lmer(), strategy_limma(), strategy_limpa(), strategy_logistf(), summary_ROPECA_median_p.scaled(), unregister_facade(), vcov.rfit_prolfqua()

Super class

prolfqua::ContrastsInterface -> ContrastsLimpaFacade

Public fields

model

ModelLimma object (from build_model_limpa)

contrast

ContrastsLimma object

.lfqdata

stored reference to input LFQData

.contrast_names

names of the requested contrasts

Methods

Inherited methods


Method new()

initialize

Usage

ContrastsLimpaFacade$new(
  lfqdata,
  modelstr,
  contrasts,
  plot = FALSE,
  span = NULL,
  ...
)

Arguments

lfqdata

aggregated LFQData. If config$opt_se is set (e.g. from AggregateLimpa), the SE column is used as a vooma precision-weight predictor; otherwise vooma is fit without an external predictor.

modelstr

model formula string (e.g. "~ group_")

contrasts

named character vector of contrasts

plot

logical; if TRUE, plot the vooma mean-variance trend

span

lowess smoother span (NULL = auto)

...

passed to strategy_limpa (e.g. trend, robust)


Method get_contrasts()

get contrast results (rows with NA diff are filtered out)

Usage

ContrastsLimpaFacade$get_contrasts(...)

Arguments

...

passed to ContrastsLimma$get_contrasts


Method get_missing()

get protein x contrast pairs that could not be estimated

Usage

ContrastsLimpaFacade$get_missing()


Method get_Plotter()

get ContrastsPlotter

Usage

ContrastsLimpaFacade$get_Plotter(...)

Arguments

...

passed to ContrastsLimma$get_Plotter


Method to_wide()

convert results to wide format

Usage

ContrastsLimpaFacade$to_wide(...)

Arguments

...

passed to ContrastsLimma$to_wide


Method clone()

The objects of this class are cloneable with this method.

Usage

ContrastsLimpaFacade$clone(deep = FALSE)

Arguments

deep

Whether to make a deep clone.

Examples

istar <- prolfqua::sim_lfq_data_peptide_config()
#> creating sampleName from file_name column
#> completing cases
#> completing cases done
#> setup done
lfqdata <- LFQData$new(istar$data, istar$config)
lfqdata <- lfqdata$get_Transformer()$log2()$lfq
#> Column added : log2_abundance
agg <- AggregateLimpa$new(lfqdata, "protein")
lfq_agg <- agg$aggregate()
#> completing cases
contrasts <- c("A_vs_Ctrl" = "group_A - group_Ctrl")
fa <- ContrastsLimpaFacade$new(lfq_agg, "~ group_", contrasts)
head(fa$get_contrasts())
#> # A tibble: 6 × 14
#>   facade modelName protein_Id  contrast     diff       FDR std.error statistic
#>   <chr>  <chr>     <chr>       <chr>       <dbl>     <dbl>     <dbl>     <dbl>
#> 1 limpa  limpa     0EfVhX~0087 A_vs_Ctrl -0.0244 0.407        0.0283    -0.862
#> 2 limpa  limpa     7cbcrd~5725 A_vs_Ctrl  0.725  0.00458      0.185      3.91 
#> 3 limpa  limpa     9VUkAq~4703 A_vs_Ctrl -0.572  0.000276     0.0991    -5.78 
#> 4 limpa  limpa     BEJI92~5282 A_vs_Ctrl  0.236  0.0138       0.0739     3.19 
#> 5 limpa  limpa     CGzoYe~2147 A_vs_Ctrl -0.296  0.146        0.175     -1.70 
#> 6 limpa  limpa     DoWup2~5896 A_vs_Ctrl  0.282  0.0000889    0.0417     6.77 
#> # ℹ 6 more variables: p.value <dbl>, sigma <dbl>, df <dbl>, conf.low <dbl>,
#> #   conf.high <dbl>, avgAbd <dbl>