calculateRelatednessCn | R Documentation |
Calculates the relatedness scores and (optionally) p-values for paired tumours from copy number data
calculateRelatednessCn(
segmentTable,
pairs,
reference = NULL,
cnType = c("alleleSpecific", "VCF"),
excludeChromosomes = "Y",
maxgap = NULL
)
segmentTable |
A segment table generated by the readAlleleSpecific or readVCFCn functions. |
pairs |
A table of paired samples from the dataset, to test for relatedness. |
reference |
A numeric vector of pair scores comprising the reference distribution, generated from the |
cnType |
The type of copy number data provided. Currently supported options are a custom allele specific data format, and standard copy number VCF files. |
excludeChromosomes |
The name(s) of any chromosomes to be excluded. |
maxgap |
The maximum gap between two breakpoints for them to be considered concordant. If unspecified, it is automatically set to 5 times the average interprobe distance of the assay. |
A data frame listing the tumour pairs contained in pairs
, their relatedness scores and p-values for relatedness.
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