View source: R/apply.ns.cna.thresh.R
apply.ns.cna.thresh | R Documentation |
Determine the copy number values from count ratios using pre-defined thresholds
apply.ns.cna.thresh(ratio.data, cna.thresh = c(0.4, 1.5, 2.5, 3.5))
ratio.data |
A gene by sample data-frame of tumour:normal ratios. See output of NanoStringNormCNV:::get.tumour.normal.ratio |
cna.thresh |
A 4-element vector with the tumour-normal thresholds to call homozygous deletions, heterozygous deletions, single copy gains, and multi-copy gains. Default values (0.4, 1.5, 2.5, 3.5) are derived from NanoString recommendations. |
Determine the copy number values (0, 1, 2, 3, 4) of each probe from raw tumour:normal count ratios using pre-defined thresholds.
A gene by sample data-frame of copy number values
Cindy Yao and Emilie Lalonde
See NanoString website for PDFs on analysis guidelines: https://www.nanostring.com/support/product-support/support-documentation
The NanoString assay is described in the paper: Fortina, P. & Surrey, S. Digital mRNA profiling. Nature Biotechnology 26, 293-294 (2008).
NanoStringNormCNV:::apply.kd.cna.thresh
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