| saasCNV-package | Somatic Copy Number Alteration Analysis Using Sequencing and SNP Array Data |
| BAF2mBAF | Internal Functions and Data |
| check.overlap | Internal Functions and Data |
| cnv.call | CNV Calling from Sequencing Data |
| cnv.data | Construct Data Frame for CNV Inference with NGS Data |
| cnv.data.chr | Internal Functions and Data |
| compute.baseline | Internal Functions and Data |
| compute.baseline.manual | Internal Functions and Data |
| compute.var | Internal Functions and Data |
| computeBeta | Internal Functions and Data |
| computeMoments | Internal Functions and Data |
| computeTiltDirect | Internal Functions and Data |
| ComputeZ.fromS.R | Internal Functions and Data |
| ComputeZ.fromS.R.partial | Internal Functions and Data |
| computeZ.onechange | Internal Functions and Data |
| computeZ.onechange.sample | Internal Functions and Data |
| computeZ.squarewave.sample | Internal Functions and Data |
| dchi | Internal Functions and Data |
| delta.sd | Internal Functions and Data |
| diagnosis.cluster.plot | Visualize Genome-Wide SCNA Profile in 2D Cluster Plot |
| diagnosis.QQ.plot | Internal Functions and Data |
| diagnosis.seg.plot.chr | Visualize Segmentation Results for Diagnosis |
| fcompute.max.Z | Internal Functions and Data |
| fmscbs | Internal Functions and Data |
| fscan.max | Internal Functions and Data |
| GC.adjust | GC Content Adjustment |
| genome.wide.plot | Visualize Genome-Wide SCNA Profile |
| getCutoffMultisampleWeightedChisq | Internal Functions and Data |
| impute.missing.data | Internal Functions and Data |
| joint.segmentation | Joint Segmentation on log2ratio and log2mBAF Dimensions |
| matrix.max | Internal Functions and Data |
| merging.segments | Merge Adjacent Segments |
| merging.segments.chr | Internal Functions and Data |
| Mode | Internal Functions and Data |
| mscbs.classify | Internal Functions and Data |
| NGS.CNV | CNV Analysis Pipeline for WGS and WES Data |
| pmarg.sumweightedchisq | Internal Functions and Data |
| pvalueMultisampleWeightedChisq | Internal Functions and Data |
| reannotate.CNV.res | Gene Annotation |
| saasCNV | Somatic Copy Number Alteration Analysis Using Sequencing and SNP Array Data |
| seg.summary | Internal Functions and Data |
| seq.cnv | Internal Functions and Data |
| seq.data | Internal Functions and Data |
| seq.segs | Internal Functions and Data |
| seq.segs.merge | Internal Functions and Data |
| SNP.CNV | CNV Analysis Pipeline for SNP array Data |
| snp.cnv | Internal Functions and Data |
| snp.cnv.anno | Internal Functions and Data |
| snp.cnv.data | Construct Data Frame for CNV Inference with SNP Array Data |
| snp.cnv.refine | Internal Functions and Data |
| snp.cnv.refine.anno | Internal Functions and Data |
| snp.data | Internal Functions and Data |
| snp.refine.boundary | Refine Segment Boundaries |
| snp.segs | Internal Functions and Data |
| snp.segs.merge | Internal Functions and Data |
| snp_table | Internal Functions and Data |
| vcf2txt | Covert VCF File to A Data Frame |
| vcf_table | Internal Functions and Data |
| vu | Internal Functions and Data |