| TitanCNA-package | TITAN: Subclonal copy number and LOH prediction whole genome sequencing of tumours |
| computeSDbwIndex | Compute the S_Dbw Validity Index for 'TitanCNA' model selection |
| convergeParams | TITAN EM trained results for an example dataset |
| correctIntegerCN | Compute purity and ploidy corrected log ratios; recompute integer CN for high-level amplifications. |
| correctReadDepth | Correct GC content and mappability biases in sequencing data read counts |
| data | TITAN EM trained results for an example dataset |
| EMresults | TITAN EM trained results for an example dataset |
| filterData | Filter list object based on read depth and missing data and returns a filtered data.table object. |
| getHaplotypesFromVCF | Function to load tumour allele counts from a text file or data.frame and returns a data.table ('loadHaplotypeAlleleCounts'). Function to load phased heterozygous sites from a VCF file ('getHaplotypesFromVCF') |
| getPositionOverlap | Function to assign values to given chromosome-position that overlaps a list of chromosomal segments |
| loadAlleleCounts | Function to load tumour allele counts from a text file or data.frame and returns a data.table. |
| loadBXcountsFromBEDDir | Function to load tumour allele counts from a text file or data.frame and returns a data.table ('loadHaplotypeAlleleCounts'). Function to load phased heterozygous sites from a VCF file ('getHaplotypesFromVCF') |
| loadDefaultParameters | Load TITAN parameters |
| loadHaplotypeAlleleCounts | Function to load tumour allele counts from a text file or data.frame and returns a data.table ('loadHaplotypeAlleleCounts'). Function to load phased heterozygous sites from a VCF file ('getHaplotypesFromVCF') |
| outputModelParameters | Formatting and printing 'TitanCNA' results. |
| outputTitanResults | Formatting and printing 'TitanCNA' results. |
| outputTitanSegments | Formatting and printing 'TitanCNA' results. |
| plotAllelicRatio | Plotting functions for 'TitanCNA' results. |
| plotClonalFrequency | Plotting functions for 'TitanCNA' results. |
| plotCNlogRByChr | Plotting functions for 'TitanCNA' results. |
| plotHaplotypeFraction | Plotting functions for 'TitanCNA' results. |
| plotSegmentMedians | Plotting functions for 'TitanCNA' results. |
| plotSubcloneProfiles | Plotting functions for 'TitanCNA' results. |
| runEMclonalCN | Function to run the Expectation Maximization Algorithm in 'TitanCNA'. |
| setGenomeStyle | Function to load tumour allele counts from a text file or data.frame and returns a data.table. |
| TitanCNA | TITAN: Subclonal copy number and LOH prediction whole genome sequencing of tumours |
| TitanCNA-dataset | TITAN EM trained results for an example dataset |
| viterbiClonalCN | Function to run the Viterbi algorithm for 'TitanCNA'. |
| wigToRangedData | WIG Import Functions |