Files in caravagnalab/CNAqc
CNAqc - Copy Number Analysis quality check

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.Rbuildignore
.github/.gitignore
.github/workflows/R-CMD-check.yaml
.github/workflows/pkgdown.yaml
.gitignore
DESCRIPTION
DriverDBv3.rda
LICENSE
LICENSE.md
NAMESPACE
NEWS
R/.Rapp.history
R/CNAqc-package.R R/advanced_phasing.R R/analyze_peaks.R R/annotate_variants.R R/assign_sbs_contexts.R R/auto_tolerance.R R/blank_genome.R R/compute_CCF.R R/data.R R/detect_arm_overfragmentation.R R/detect_wg_overfragmentation.R R/drivers.R R/eplot.R R/equations.R R/evo_dynamics.R R/fortify.R R/general_peaks.R R/get_prevalent_karyotype.R R/get_reference.R R/getters.R R/init.R R/inspect_segment.R R/maf.R R/maf_utils.R R/map_mutations.R R/mutation_multiplicity.R R/parse_Battenberg.R R/peak_algorithms.R R/peak_detector.R R/pipelines.R R/plot_CCF.R R/plot_arm_fragmentation.R R/plot_cohort_CNA.R R/plot_data_histogram.R R/plot_genome_wide_mutations.R R/plot_icon_cna.R R/plot_karyotypes.R R/plot_multisample_CNA.R R/plot_multisample_driversA.R R/plot_peaks_analysis.R R/plot_qc.R R/plot_segment_size_distribution.R R/plot_segments.R R/plot_smoothing.R R/prepare_input_data.R R/print.cnaqc.R R/smooth_segments.R
R/subclonal_peaks.R
R/subsample.R R/utils-pipe.R R/utils_CCF.R R/utils_fragmentation.R R/utils_plot.R R/vaf_functions.R R/vep.R R/zzz.R README.Rmd README.md
_config.yml
_pkgdown.yml
data/chr_coordinates_GRCh38.rda
data/chr_coordinates_hg19.rda
data/example_PCAWG.rda
data/example_dataset_CNAqc.rda
data/fpr_test.rda
data/gene_coordinates_GRCh38.rda
data/gene_coordinates_hg19.rda
data/intogen_drivers.rda
docs/404.html
docs/LICENSE-text.html
docs/LICENSE.html
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docs/articles/CNAqc.html
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docs/reference/CCF.html
docs/reference/CNA.html
docs/reference/CNA_gene.html
docs/reference/CNAqc-package.html
docs/reference/DriverDBv3.html
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docs/reference/SBS.html
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docs/reference/Sequenza_CNAqc.html
docs/reference/analyze_peaks.html
docs/reference/annotate_variants.html
docs/reference/as_maftools_cohort.html
docs/reference/as_maftools_obj.html
docs/reference/augment_with_maf.html
docs/reference/augment_with_vep.html
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docs/reference/boostDM_drivers.html
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docs/reference/chr_coordinates_hg19.html
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docs/reference/compute_CCF.html
docs/reference/detect_arm_overfragmentation.html
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docs/reference/example_dataset_CNAqc.html
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docs/reference/fpr_test.html
docs/reference/gene_coordinates_GRCh38.html
docs/reference/gene_coordinates_hg19.html
docs/reference/get_PASS_percentage.html
docs/reference/get_drivers.html
docs/reference/index.html
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docs/reference/inspect_segment.html
docs/reference/intogen_drivers.html
docs/reference/parse_Battenberg.html
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docs/reference/print.cnaqc.html
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docs/reference/split_by_chromosome.html
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docs/reference/subset_by_minimum_CCF.html
docs/reference/subset_by_segment_karyotype.html
docs/reference/subset_by_segment_minmutations.html
docs/reference/subset_by_segment_totalcn.html
docs/reference/subset_snvs.html
docs/reference/wt_mutant_alleles.html
docs/sitemap.xml
logo.png
man/CCF.Rd man/CNA.Rd man/CNA_gene.Rd man/CNAqc-package.Rd man/Mutations.Rd man/SBS.Rd man/SBS_counts.Rd man/Sequenza_CNAqc.Rd man/analyze_peaks.Rd man/annotate_variants.Rd man/as_maftools_cohort.Rd man/as_maftools_obj.Rd man/augment_with_maf.Rd man/augment_with_vep.Rd man/auto_tolerance.Rd man/chr_coordinates_GRCh38.Rd man/chr_coordinates_hg19.Rd man/compute_CCF.Rd man/detect_arm_overfragmentation.Rd man/example_PCAWG.Rd man/example_dataset_CNAqc.Rd man/fpr_test.Rd man/gene_coordinates_GRCh38.Rd man/gene_coordinates_hg19.Rd man/get_PASS_percentage.Rd man/get_drivers.Rd man/init.Rd man/inspect_segment.Rd man/intogen_drivers.Rd man/parse_Battenberg.Rd man/pipe.Rd man/plot.cnaqc.Rd man/plot_CCF.Rd man/plot_SBS.Rd man/plot_arm_fragmentation.Rd man/plot_data_histogram.Rd man/plot_gw_ccf.Rd man/plot_gw_counts.Rd man/plot_gw_depth.Rd man/plot_gw_vaf.Rd man/plot_icon_CNA.Rd man/plot_karyotypes.Rd man/plot_multisample_CNA.Rd man/plot_peaks_analysis.Rd man/plot_qc.Rd man/plot_segment_size_distribution.Rd man/plot_segments.Rd man/plot_smoothing.Rd man/print.cnaqc.Rd man/smooth_segments.Rd man/split_by_chromosome.Rd man/subsample.Rd man/subset_by_minimum_CCF.Rd man/subset_by_segment_karyotype.Rd man/subset_by_segment_minmutations.Rd man/subset_by_segment_totalcn.Rd man/subset_snvs.Rd man/wt_mutant_alleles.Rd
nobuild/Exome_genes.zip
nobuild/annotate_drivers.R nobuild/annotate_genes_from_locations.R
nobuild/boostDM_drivers.rda
nobuild/create_drivers_list.R nobuild/data.R nobuild/ensemble_exomes.R
nobuild/exones_GRCh38.rda
nobuild/exones_hg19.rda
nobuild/fix_peak_analysis.R
nobuild/intogen_ttypes.rda
nobuild/mutation_download_tab.txt
nobuild/package_template.R nobuild/plot_cohort_CNA.R nobuild/sampler.R
pkgdown/favicon/apple-touch-icon-120x120.png
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vignettes/.gitignore
vignettes/CNAqc.Rmd vignettes/a1_Introduction.Rmd vignettes/a2_Plots.Rmd vignettes/a3_peaks_detection.Rmd vignettes/a4_ccf_computation.Rmd vignettes/a5_smoothing.Rmd vignettes/a6_fragmentation.Rmd vignettes/a7_example_MSeq.Rmd vignettes/a8_annotate_variants.Rmd vignettes/a9_automatic.Rmd
vignettes/logo_summary.png
vignettes/peaks.png
vignettes/sqz_pipe.png
caravagnalab/CNAqc documentation built on Oct. 31, 2024, 3:54 a.m.