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 |