Data input, classes and operationRead genomic variation data as an R object and more. |
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Read Absolute Copy Number Profile |
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Read Absolute Copy Number Profile from Sequenza Result Directory |
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Read Copy Number Data from ASCAT Result Files |
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Read MAF Files |
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Read Structural Variation Data as RS object |
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Read VCF Files as MAF Object |
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Read UCSC Xena Variant Format Data as MAF Object |
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Class CopyNumber |
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Class MAF |
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Subsetting CopyNumber object |
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Core pipeline 1 - de novo signature identificationIdentify signatures from genomic variation profile. After reading data, the following functions construct the standard pipeline for most users. |
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Tally a Genomic Alteration Object |
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Handle Hypermutant Samples |
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Estimate Signature Number |
An Unified Interface to Extract Signatures |
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Extract Signatures through NMF |
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Extract Signatures through the Automatic Relevance Determination Technique |
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Extract Signatures with SigProfiler |
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A Best Practice for Signature Extraction and Exposure (Activity) Attribution |
Core pipeline 2 - signature exposure fitting and optimizationQuantify exposure in at least one sample with reference signatures. It can also be used to optimize signature exposure from pipeline 1 and analyze exposure instability. |
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Tally a Genomic Alteration Object |
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Handle Hypermutant Samples |
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Obtain Signature Index for Cancer Types |
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Fit Signature Exposures with Linear Combination Decomposition |
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Obtain Bootstrap Distribution of Signature Exposures of a Certain Tumor Sample |
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Exposure Instability Analysis of Signature Exposures with Bootstrapping |
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Report P Values from bootstrap Results |
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Signature visualizationShow signature profile and exposure. |
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Show Alteration Catalogue Profile |
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Show Signature Profile |
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Show Signature Profile with Loop Way |
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Show Signature Profile with Heatmap |
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Plot Signature Exposure |
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Show Signature Information in Web Browser |
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Plot Reference (Mainly COSMIC) Signature Profile |
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Show Signature Consensus Map |
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Fit and bootstrap visualizationShow signature fit and bootstrap analysis results. |
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Show Signature Fit Result |
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Show Signature Bootstrap Analysis Results |
Output analysis results to local machineSave results and plots as files. For automatic analysis, please use sigflow. |
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Output Tally Result in Barplots |
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Output Signature Results |
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Output Signature Fitting Results |
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Output Signature Bootstrap Fitting Results |
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Signature object operationObtain or modify |
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Obtain or Modify Signature Information |
Signature analysis and corresponding visualizationAnalyze signatures and output the result to visualization. |
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Calculate Similarity between Identified Signatures and Reference Signatures |
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Get Reconstructed Profile Cosine Similarity, RSS, etc. |
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Get Signature Exposure from 'Signature' Object |
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Calculate Association between Signature Exposures and Other Features |
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Get Tidy Signature Association Results |
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A Simple and General Way for Association Analysis |
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Draw Corrplot for Signature Exposures and Other Features |
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Show Signature Contribution in Clusters |
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Get Sample Groups from Signature Decomposition Information |
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Get Comparison Result between Signature Groups |
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Plot Group Comparison Result |
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General Group Enrichment Analysis |
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Show Group Enrichment Result |
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Group Enrichment Analysis with Subsets |
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Show Groupped Variable Distribution |
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Map Groups using Sankey |
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Performs Strand Bias Enrichment Analysis for a Given Sample-by-Component Matrix |
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Simulation Analysis |
Get Shannon Diversity Index for Signatures |
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Package datasetsDatasets used for signature identification and analysis (some stored in |
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A List of Simulated SBS-96 Catalog Matrix |
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Classification Table of Copy Number Features Devised by Wang et al. for Method 'W' |
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Location of Centromeres at Genome Build hg19 |
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Location of Centromeres at Genome Build hg38 |
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Location of Centromeres at Genome Build T2T |
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Location of Centromeres at Genome Build mm10 |
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Location of Centromeres at Genome Build mm9 |
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Chromosome Size of Genome Build hg19 |
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Chromosome Size of Genome Build hg38 |
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Chromosome Size of Genome Build T2T |
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Chromosome Size of Genome Build mm10 |
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Chromosome Size of Genome Build mm9 |
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Location of Chromosome Cytobands at Genome Build hg19 |
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Location of Chromosome Cytobands at Genome Build hg38 |
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Location of Chromosome Cytobands at Genome Build T2T |
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Location of Chromosome Cytobands at Genome Build mm10 |
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Location of Chromosome Cytobands at Genome Build mm9 |
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Merged Transcript Location at Genome Build hg19 |
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Merged Transcript Location at Genome Build hg38 |
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Merged Transcript Location at Genome Build T2T |
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Merged Transcript Location at Genome Build mm10 |
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Merged Transcript Location at Genome Build mm9 |
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HelpersHelper functions used in the sigminer package. |
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Get Curated Reference Signature Database |
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Convert Signatures between different Genomic Distribution of Components |
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Get Genome Annotation |
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Get Specified Bayesian NMF Result from Run |
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Get Adjust P Values from Group Comparison |
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Set Color Style for Plotting |
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Add Horizontal Arrow with Text Label to a ggplot |
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Add Text Labels to a ggplot |
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Calculate Cosine Measures |
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Get CNV Frequency Table |
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Same Size Clustering |
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Get Overlap Size between Interval x and y |
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Copy number analysis and visualizationFunctions for analyzing copy number data and visualization. |
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Transform Copy Number Table |
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Get Ploidy from Absolute Copy Number Profile |
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Get Aneuploidy Score from Copy Number Profile |
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Get proportions of pLOH score from Allele Specific Copy Number Profile |
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Score Copy Number Profile |
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Show Sample Copy Number Profile |
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Show Copy Number Profile in Circos |
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Show Summary Copy Number Profile for Sample Groups |
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Show Copy Number Variation Frequency Profile with Circos |
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Show Copy Number Distribution either by Length or Chromosome |
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Show Copy Number Feature Distributions |
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Show Copy Number Components |
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Extra documentationExtra function and introduction. |
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Say Hello to Users |
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sigminer: Extract, Analyze and Visualize Signatures for Genomic Variations |