Skip to contents

Limpa contrast analysis facade for nested input

Limpa contrast analysis facade for nested input

Value

An R6 class generator.

Details

Encapsulates the full precursor -> protein pipeline: AggregateLimpa -> strategy_limpa -> build_model_limpa -> ContrastsLimma.

Takes nested (precursor/peptide-level) LFQData, runs limpa's DPC-based aggregation internally to produce protein-level expression with posterior standard errors, then fits a vooma model with imputation-aware precision weights.

For protein-level input that was already aggregated upstream via AggregateLimpa, use ContrastsLimpaFacade instead.

See also

Other modelling: AnovaExtractor, Contrasts, ContrastsDEqMSFacade, ContrastsDEqMSVoomFacade, ContrastsFirth, ContrastsFirthFacade, ContrastsFirthNestedFacade, ContrastsLMFacade, ContrastsLMImputeFacade, ContrastsLMMissingFacade, ContrastsLimma, ContrastsLimmaFacade, ContrastsLimmaImputeFacade, ContrastsLimmaVoomFacade, ContrastsLimmaVoomImputeFacade, ContrastsLimpaFacade, ContrastsLmerNestedFacade, ContrastsMissing, ContrastsModerated, ContrastsModeratedDEqMS, ContrastsPlotter, ContrastsRLMFacade, ContrastsROPECA, ContrastsROPECANestedFacade, ContrastsTable, INTERNAL_FUNCTIONS_BY_FAMILY, LR_test(), Model, ModelFirth, ModelLimma, StrategyLM, StrategyLimma, StrategyLimpa, StrategyLmer, StrategyLogistf, StrategyRLM, 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(), 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(), 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()

Super class

prolfqua::ContrastsInterface -> ContrastsLimpaNestedFacade

Public fields

model

ModelLimma object (from build_model_limpa)

contrast

ContrastsLimma object

.lfqdata

stored reference to the aggregated protein-level LFQData

.lfqdata_nested

stored reference to the original nested input

.contrast_names

names of the requested contrasts

Methods

Inherited methods


Method new()

initialize

Usage

ContrastsLimpaNestedFacade$new(
  lfqdata,
  modelstr,
  contrasts,
  prefix = "protein",
  dpc_slope = 0.8,
  plot = FALSE,
  span = NULL,
  ...
)

Arguments

lfqdata

nested LFQData (precursor/peptide-level, log2-transformed)

modelstr

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

contrasts

named character vector of contrasts

prefix

prefix for the aggregated hierarchy level (default "protein")

dpc_slope

DPC slope parameter passed to AggregateLimpa (default 0.8)

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

ContrastsLimpaNestedFacade$get_contrasts(...)

Arguments

...

passed to ContrastsLimma$get_contrasts


Method get_missing()

get protein x contrast pairs that could not be estimated

Usage

ContrastsLimpaNestedFacade$get_missing()


Method get_Plotter()

get ContrastsPlotter

Usage

ContrastsLimpaNestedFacade$get_Plotter(...)

Arguments

...

passed to ContrastsLimma$get_Plotter


Method to_wide()

convert results to wide format

Usage

ContrastsLimpaNestedFacade$to_wide(...)

Arguments

...

passed to ContrastsLimma$to_wide


Method clone()

The objects of this class are cloneable with this method.

Usage

ContrastsLimpaNestedFacade$clone(deep = FALSE)

Arguments

deep

Whether to make a deep clone.

Examples

if (requireNamespace("limpa", quietly = TRUE)) {
  istar <- prolfqua::sim_lfq_data_peptide_config(Nprot = 10)
  lfqdata <- LFQData$new(istar$data, istar$config)
  lfqdata <- lfqdata$get_Transformer()$log2()$lfq
  contrasts <- c("A_vs_Ctrl" = "group_A - group_Ctrl")
  fa <- ContrastsLimpaNestedFacade$new(lfqdata, "~ group_", contrasts)
  head(fa$get_contrasts())
}
#> creating sampleName from file_name column
#> completing cases
#> completing cases done
#> setup done
#> Column added : log2_abundance
#> # A tibble: 6 × 14
#>   facade       modelName protein_Id contrast    diff     FDR std.error statistic
#>   <chr>        <chr>     <chr>      <chr>      <dbl>   <dbl>     <dbl>     <dbl>
#> 1 limpa_nested limpa     0EfVhX~00… A_vs_Ct… -0.0244 4.07e-1    0.0283    -0.862
#> 2 limpa_nested limpa     7cbcrd~57… A_vs_Ct…  0.725  4.58e-3    0.185      3.91 
#> 3 limpa_nested limpa     9VUkAq~47… A_vs_Ct… -0.572  2.76e-4    0.0991    -5.78 
#> 4 limpa_nested limpa     BEJI92~52… A_vs_Ct…  0.236  1.38e-2    0.0739     3.19 
#> 5 limpa_nested limpa     CGzoYe~21… A_vs_Ct… -0.296  1.46e-1    0.175     -1.70 
#> 6 limpa_nested limpa     DoWup2~58… A_vs_Ct…  0.282  8.89e-5    0.0417     6.77 
#> # ℹ 6 more variables: p.value <dbl>, sigma <dbl>, df <dbl>, conf.low <dbl>,
#> #   conf.high <dbl>, avgAbd <dbl>