A B C D E F G H L M N P R S T V Y
add_annotation | Add information to an annotation data structure |
add_as_fist_to_list | Add an element as first entry to a list |
aggregate_exposures_by_category | Aggregate exposures by category |
AlexCosmicArtif_sigInd_df | Data for mutational signatures |
AlexCosmicArtif_sig_df | Data for mutational signatures |
AlexCosmicValid_sigInd_df | Data for mutational signatures |
AlexCosmicValid_sig_df | Data for mutational signatures |
AlexInitialArtif_sigInd_df | Data for mutational signatures |
AlexInitialArtif_sig_df | Data for mutational signatures |
AlexInitialValid_sigInd_df | Data for mutational signatures |
AlexInitialValid_sig_df | Data for mutational signatures |
annotate_intermut_dist_cohort | Annotate the intermutation distance of variants cohort-wide |
annotate_intermut_dist_PID | Annotate the intermutation distance of variants per PID |
annotation_exposures_barplot | Plot the exposures of a cohort with different layers of annotation |
annotation_exposures_list_barplot | Plot the exposures of a cohort with different layers of annotation for SNV and INDEL signatures |
annotation_heatmap_exposures | Heatmap to cluster the PIDs on their signature exposures (ComplexHeatmap) |
attribute_nucleotide_exchanges | Attribute the nucleotide exchange for an SNV |
attribute_sequence_contex_indel | Attribution of sequence context and size for an INDEL |
attribution_of_indels | Attribution of variant into one onf the 83 INDEL categories |
average_over_present | Useful functions on data frames |
build_gene_list_for_pathway | Build a gene list for a given pathway name |
chosen_AlexInitialArtif_sigInd_df | Test and example data |
chosen_signatures_indices_df | Test and example data |
classify_indels | INDEL function V1 - not compartible with AlexandrovSignatures |
compare_exposures | Compares alternative exposures |
compare_expousre_sets | Compare two sets of exposures by cosine distance |
compare_sets | Compare two sets of signatures by cosine distance |
compare_SMCs | Compare all strata from different stratifications |
compare_to_catalogues | Compare one mutational catalogue to reference mutational catalogues |
complex_heatmap_exposures | Heatmap to cluster the PIDs on their signature exposures (ComplexHeatmap) |
computeLogLik | Compute the loglikelihood |
compute_comparison_stat_df | Extract statistical measures for entity comparison |
confidence_indel_calulation | Wrapper to compute confidence intervals for SNV and INDEL signatures of a cohort or single-sample |
confidence_indel_only_calulation | Wrapper to compute confidence intervals for only INDEL signatures. |
confIntExp | Compute confidence intervals |
correct_rounded | Readjust the vector to it's original norm after rounding |
cosineDist | Compute the cosine distance of two vectors |
cosineMatchDist | Compute an altered cosine distance of two vectors |
COSMIC_subgroups_df | Test and example data |
create_indel_mutation_catalogue_from_df | Wrapper to create an INDEL mutational catalog from a vlf-like data frame |
create_indel_mut_cat_from_df | Create a Mutational catalog from a data frame |
create_mutation_catalogue_from_df | Create a Mutational Catalogue from a data frame |
create_mutation_catalogue_from_VR | Create a Mutational Catalogue from a VRanges Object |
cutoffCosmicArtif_abs_df | Cutoffs for a supervised analysis of mutational signatures. |
cutoffCosmicArtif_rel_df | Cutoffs for a supervised analysis of mutational signatures. |
cutoffCosmicValid_abs_df | Cutoffs for a supervised analysis of mutational signatures. |
cutoffCosmicValid_rel_df | Cutoffs for a supervised analysis of mutational signatures. |
cutoffInitialArtif_abs_df | Cutoffs for a supervised analysis of mutational signatures. |
cutoffInitialArtif_rel_df | Cutoffs for a supervised analysis of mutational signatures. |
cutoffInitialValid_abs_df | Cutoffs for a supervised analysis of mutational signatures. |
cutoffInitialValid_rel_df | Cutoffs for a supervised analysis of mutational signatures. |
cutoffPCAWG_ID_WGS_Pid_df | Opt. cutoffs, PCAWG SNV signatures, including artifacts |
cutoffPCAWG_SBS_WGSWES_artifPid_df | Opt. cutoffs, PCAWG SNV signatures, including artifacts |
cutoffPCAWG_SBS_WGSWES_realPid_df | Opt. cutoffs, PCAWG SNV signatures, including artifacts |
cutoffs | Cutoffs for a supervised analysis of mutational signatures. |
cutoffs_pcawg | Opt. cutoffs, PCAWG SNV signatures, including artifacts |
cut_breaks_as_intervals | Wrapper for cut |
deriveSigInd_df | Derive a signature_indices_df object |
disambiguateVector | Disambiguate a vector |
enrichSigs | Compare to background distribution |
exampleINDEL_YAPSA | Data structures used in examples, Indel tests and the Indel signature vignette of the YAPSA package. |
exampleYAPSA | Test and example data |
exchange_colour_vector | Colours codes for displaying SNVs |
exome_mutCatRaw_df | Example mutational catalog for the exome vignette |
exposures_barplot | Wrapper for enhanced_barplot |
extract_names_from_gene_list | Return gene names from gene lists |
find_affected_PIDs | Find samples affected |
GenomeOfNl_raw | Example data for the Indel vignette |
getSequenceContext | Extracts the sequence context up and downstream of a nucleotide position |
get_extreme_PIDs | Return those PIDs which have an extreme pattern for signature exposure |
hclust_exposures | Cluster the PIDs according to their signature exposures |
LCD | Linear Combination Decomposition |
LCD_complex_cutoff | LCD with a signature-specific cutoff on exposures |
LCD_complex_cutoff_combined | LCD with a signature-specific cutoff on exposures |
LCD_complex_cutoff_consensus | LCD with a signature-specific cutoff on exposures |
LCD_complex_cutoff_perPID | LCD with a signature-specific cutoff on exposures |
LCD_extractCohort_callPerPID | LCD with a signature-specific cutoff on exposures |
LCD_SMC | CD stratification analysis |
logLikelihood | Compute a loglikelihood ratio test |
lymphomaNature2013_mutCat_df | Example mutational catalog for the SNV vignette |
lymphoma_Nature2013_COSMIC_cutoff_exposures_df | Test and example data |
lymphoma_Nature2013_raw_df | Test and example data |
lymphoma_PID_df | Test and example data |
lymphoma_test_df | Test and example data |
makeVRangesFromDataFrame | Construct a VRanges Object from a data frame |
make_catalogue_strata_df | Group strata from different stratification axes |
make_comparison_matrix | Compute a similarity matrix for different strata |
make_strata_df | Group strata from different stratification axes |
make_subgroups_df | Make a custom data structure for subgroups |
melt_exposures | Generically melts exposure data frames |
merge_exposures | Merge exposure data frames |
MutCat_indel_df | Example mutational catalog for the Indel vignette |
normalizeMotifs_otherRownames | Normalize Somatic Motifs with different rownames |
normalize_df_per_dim | Useful functions on data frames |
PCAWG_SP_ID_sigInd_df | Data for PCAWG SNV signatures (COSMIC v3), including artifacts 'PCAWG_SP_SBS_sigs_Artif_df': Data frame of the signatures published by Alexandrov et al. (Biorxiv 2013) which were decomposed with the method SigProfiler. SNV signatures are labeled with SBS, single base signature. There are 67 signatures which constitute the columns, 47 of which were validated by a bayesian NFM mehtod, SignatureAnayzer. Validated signatures are SBS1-SBS26,SBS28-SBS42 and SBS44. SBS7 is split up into 7 a/b/c and d. SBS10 ans SBS17 are both split up into a and b. Resulting in a 47 validated sigantures. Please note, unlike the paper by Alexandrov et al. (Biorxiv 2018) the data sets do not contain a SBS84 and SBS85 as not all were availiablt to perfom supervised signature analysis. In total there are 96 different features and therefore 96 rows when dealing with a trinucleotide context. |
PCAWG_SP_ID_sigs_df | Data for PCAWG SNV signatures (COSMIC v3), including artifacts 'PCAWG_SP_SBS_sigs_Artif_df': Data frame of the signatures published by Alexandrov et al. (Biorxiv 2013) which were decomposed with the method SigProfiler. SNV signatures are labeled with SBS, single base signature. There are 67 signatures which constitute the columns, 47 of which were validated by a bayesian NFM mehtod, SignatureAnayzer. Validated signatures are SBS1-SBS26,SBS28-SBS42 and SBS44. SBS7 is split up into 7 a/b/c and d. SBS10 ans SBS17 are both split up into a and b. Resulting in a 47 validated sigantures. Please note, unlike the paper by Alexandrov et al. (Biorxiv 2018) the data sets do not contain a SBS84 and SBS85 as not all were availiablt to perfom supervised signature analysis. In total there are 96 different features and therefore 96 rows when dealing with a trinucleotide context. |
PCAWG_SP_SBS_sigInd_Artif_df | Data for PCAWG SNV signatures (COSMIC v3), including artifacts 'PCAWG_SP_SBS_sigs_Artif_df': Data frame of the signatures published by Alexandrov et al. (Biorxiv 2013) which were decomposed with the method SigProfiler. SNV signatures are labeled with SBS, single base signature. There are 67 signatures which constitute the columns, 47 of which were validated by a bayesian NFM mehtod, SignatureAnayzer. Validated signatures are SBS1-SBS26,SBS28-SBS42 and SBS44. SBS7 is split up into 7 a/b/c and d. SBS10 ans SBS17 are both split up into a and b. Resulting in a 47 validated sigantures. Please note, unlike the paper by Alexandrov et al. (Biorxiv 2018) the data sets do not contain a SBS84 and SBS85 as not all were availiablt to perfom supervised signature analysis. In total there are 96 different features and therefore 96 rows when dealing with a trinucleotide context. |
PCAWG_SP_SBS_sigInd_Real_df | Data for PCAWG SNV signatures (COSMIC v3), including artifacts 'PCAWG_SP_SBS_sigs_Artif_df': Data frame of the signatures published by Alexandrov et al. (Biorxiv 2013) which were decomposed with the method SigProfiler. SNV signatures are labeled with SBS, single base signature. There are 67 signatures which constitute the columns, 47 of which were validated by a bayesian NFM mehtod, SignatureAnayzer. Validated signatures are SBS1-SBS26,SBS28-SBS42 and SBS44. SBS7 is split up into 7 a/b/c and d. SBS10 ans SBS17 are both split up into a and b. Resulting in a 47 validated sigantures. Please note, unlike the paper by Alexandrov et al. (Biorxiv 2018) the data sets do not contain a SBS84 and SBS85 as not all were availiablt to perfom supervised signature analysis. In total there are 96 different features and therefore 96 rows when dealing with a trinucleotide context. |
PCAWG_SP_SBS_sigs_Artif_df | Data for PCAWG SNV signatures (COSMIC v3), including artifacts 'PCAWG_SP_SBS_sigs_Artif_df': Data frame of the signatures published by Alexandrov et al. (Biorxiv 2013) which were decomposed with the method SigProfiler. SNV signatures are labeled with SBS, single base signature. There are 67 signatures which constitute the columns, 47 of which were validated by a bayesian NFM mehtod, SignatureAnayzer. Validated signatures are SBS1-SBS26,SBS28-SBS42 and SBS44. SBS7 is split up into 7 a/b/c and d. SBS10 ans SBS17 are both split up into a and b. Resulting in a 47 validated sigantures. Please note, unlike the paper by Alexandrov et al. (Biorxiv 2018) the data sets do not contain a SBS84 and SBS85 as not all were availiablt to perfom supervised signature analysis. In total there are 96 different features and therefore 96 rows when dealing with a trinucleotide context. |
PCAWG_SP_SBS_sigs_Real_df | Data for PCAWG SNV signatures (COSMIC v3), including artifacts 'PCAWG_SP_SBS_sigs_Artif_df': Data frame of the signatures published by Alexandrov et al. (Biorxiv 2013) which were decomposed with the method SigProfiler. SNV signatures are labeled with SBS, single base signature. There are 67 signatures which constitute the columns, 47 of which were validated by a bayesian NFM mehtod, SignatureAnayzer. Validated signatures are SBS1-SBS26,SBS28-SBS42 and SBS44. SBS7 is split up into 7 a/b/c and d. SBS10 ans SBS17 are both split up into a and b. Resulting in a 47 validated sigantures. Please note, unlike the paper by Alexandrov et al. (Biorxiv 2018) the data sets do not contain a SBS84 and SBS85 as not all were availiablt to perfom supervised signature analysis. In total there are 96 different features and therefore 96 rows when dealing with a trinucleotide context. |
plotExchangeSpectra | Plot the spectra of nucleotide exchanges |
plotExchangeSpectra_indel | Plot the spectra of nucleotide exchanges of INDELs |
plotExposuresConfidence | Plot exposures including confidence intervals |
plotExposuresConfidence_indel | Plot exposures including confidence intervals for exposures of SNVs and INDELs |
plot_exposures | Plot the exposures of a cohort |
plot_relative_exposures | Plot the exposures of a cohort |
plot_SMC | Plot results of the Stratification of a Mutational Catalogue |
plot_strata | Plot all strata from different stratification axes together |
read_entry | Read a single vcf-like file into a single data frame |
read_list | Read a single vcf-like file into a single data frame |
relateSigs | Make unique assignments between sets of signatures |
rel_lymphoma_Nature2013_COSMIC_cutoff_exposures_df | Test and example data |
repeat_df | Create a data frame with default values |
round_precision | Round to a defined precision |
run_annotate_vcf_pl | Wrapper function to annotate addition information |
run_comparison_catalogues | Compare all strata from different stratifications |
run_comparison_general | Compare all strata from different stratifications |
run_kmer_frequency_correction | Provide comprehensive correction factors for kmer content |
run_kmer_frequency_normalization | Provide normalized correction factors for kmer content |
run_plot_strata_general | Wrapper function for 'plot_strata' |
run_SMC | Wrapper function for the Stratification of a Mutational Catalogue |
sd_over_present | Useful functions on data frames |
shapiro_if_possible | Wrapper for Shapiro test but allow for all identical values |
sigs | Data for mutational signatures |
sigs_pcawg | Data for PCAWG SNV signatures (COSMIC v3), including artifacts 'PCAWG_SP_SBS_sigs_Artif_df': Data frame of the signatures published by Alexandrov et al. (Biorxiv 2013) which were decomposed with the method SigProfiler. SNV signatures are labeled with SBS, single base signature. There are 67 signatures which constitute the columns, 47 of which were validated by a bayesian NFM mehtod, SignatureAnayzer. Validated signatures are SBS1-SBS26,SBS28-SBS42 and SBS44. SBS7 is split up into 7 a/b/c and d. SBS10 ans SBS17 are both split up into a and b. Resulting in a 47 validated sigantures. Please note, unlike the paper by Alexandrov et al. (Biorxiv 2018) the data sets do not contain a SBS84 and SBS85 as not all were availiablt to perfom supervised signature analysis. In total there are 96 different features and therefore 96 rows when dealing with a trinucleotide context. |
SMC | Stratification of a Mutational Catalogue |
SMC_perPID | Run SMC at a per sample level |
split_exposures_by_subgroups | Split an exposures data frame by subgroups |
stat_plot_subgroups | Plot averaged signature exposures per subgroup |
stat_test_SMC | Apply statistical tests to a stratification (SMC) |
stat_test_subgroups | Test for differences in average signature exposures between subgroups |
stderrmean | Compute the standard error of the mean |
stderrmean_over_present | Useful functions on data frames |
sum_over_list_of_df | Elementwise sum over a list of (numerical) data frames |
targetCapture_cor_factors | Correction factors for different target capture kits |
testSigs | Test for significance of alternative models cohort wide |
test_exposureAffected | Test significance of association |
test_gene_list_in_exposures | Test if mutated PIDs are enriched in signatures |
transform_rownames_deconstructSigs_to_YAPSA | Change rownames from one naming convention to another |
transform_rownames_MATLAB_to_R | Change rownames from one naming convention to another |
transform_rownames_nature_to_R | Change rownames from one naming convention to another |
transform_rownames_R_to_MATLAB | Change rownames from one naming convention to another |
transform_rownames_YAPSA_to_deconstructSigs | Change rownames from one naming convention to another |
translate_to_1kG | Translate chromosome names to the hg19 naming convention |
translate_to_hg19 | Translate chromosome names to the hg19 naming convention |
trellis_rainfall_plot | Create a rainfall plot in a trellis structure |
variateExp | Wrapper to compute confidence intervals for a cohort |
variateExpSingle | Wrapper for the likelihood ratio test |
YAPSA | Generate R documentation from inline comments. |