chrMerge {fcros} | R Documentation |
Using a C code for merging chromosome segments
Description
This is an internal function for using a C code while merging chromosome segments in the segmentation step.
Usage
chrMerge(nbSeg, idStart, idEnd, lBound, uBound, segVal, segProba,
fcall, L2R, nd, dm, sigma)
Arguments
nbSeg |
Number of current segments |
idStart |
Position indexes of the first probes for segments |
idEnd |
Positions indexes of the last probes for segments |
lBound |
Lower bound position for segments |
uBound |
Upper position for segments |
segVal |
Change values associated with segments |
segProba |
Probabilities associated with segments |
fcall |
Detection status associated with probes |
L2R |
Change values associated with probes |
nd |
Number of acceptable non-detection between two significant of a segment |
dm |
Average distance between two consecutive probes of the chromosome |
sigma |
Standard deviation of the residual observations, see reference |
Author(s)
Doulaye Dembele doulaye@igbmc.fr
References
Dembele D, Analysis of high biological data using their rank values, Stat Methods Med Res, accepted for publication, 2018
Examples
# data(fdata);