Description Usage Arguments Details Value Author(s) References Examples
A function to call alteration for CGH arrays using the fused lasso regresssion
1 |
CGH.Array |
numeric vector or matrix. It's the result of one or mutiiple CGH experiments. Each column is the log2 ratios returned from one array experiment and is ordered according to the gene/clones' position on the genome. Missing value should be coded as NA. |
chromosome |
numeric vector. Length should be the same as the row number of |
nucleotide.position |
numeric vector. Length should be the same as the row number of |
FL.norm |
numeric vector or matrix. Smoothed result of the reference arrays. Set to NULL (default) if the reference arrays are not available. |
FDR |
numeric value (between 0 and 1). User can use this option to control False Discovery Rate of the results. If not specified, the function will return the raw output of fused lasso regression on the target array. |
filter |
numeric vector. Length should be the same as the row number of |
missing.PlugIn |
Bollen value. If its value is TRUE, the missing values will be replaced with local averages. |
smooth.size |
numeric value, specifying the window size for carrying out the local average. The average is used only to replace the missing values. |
cghFLasso
calls copy number alterations for CGH arrays using the fused lasso regression.
The dynamic programming algorithm developed by N.A.Johnson is used for the model fitting.
an object of class cghFLasso
with components
Esti.CopyN |
data matrix reporting the estimated DNA copy numbers for seleted genes/clones of all the samples. |
CGH.Array |
data matrix reporting the raw CGH array measurements for selected genes/clones of all the samples. |
chromosome, nucleotide.position |
numeric vectors reporting the chromosome numbers and the nucleotide positions of selected genes/clones.
If |
FDR |
fdr value specified by the user. |
N. A. Johnson, R. Tibshirani and P. Wang
R. Tibshirani, M. Saunders, S. Rosset, J. Zhu and K. Knight (2004) ‘Sparsity and smoothness via the fused lasso’, J. Royal. Statist. Soc. B. (In press), available at http://www-stat.stanford.edu/~tibs/research.html.
P. Wang, Y. Kim, J. Pollack, B. Narasimhan and R. Tibshirani (2005) ‘A method for calling gains and losses in array CGH data’, Biostatistics 2005, 6: 45-58, available at http://www-stat.stanford.edu/~wp57/CGH-Miner/
R. Tibshirani and P. Wang (2007) ‘Spatial smoothing and hot spot detection using the Fused Lasso’, Biostatistics (In press), available at http://www-stat.stanford.edu/~tibs/research.html.
J. Friedman, T. Hastie. R. Tibshirani (2007) ‘Pathwise coordinate optimization and the fused lasso’.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 | library(cghFLasso)
data(CGH)
#############
### Example 1: Process one chromosome vector without using normal references.
CGH.FL.obj1<-cghFLasso(CGH$GBM.y)
plot(CGH.FL.obj1, index=1, type="Lines")
#############
### Example 2: Process a group of CGH arrays and use normal reference arrays.
Normal.FL<-cghFLasso.ref(CGH$NormalArray, chromosome=CGH$chromosome)
Disease.FL<-cghFLasso(CGH$DiseaseArray, chromosome=CGH$chromosome, nucleotide.position=CGH$nucposition, FL.norm=Normal.FL, FDR=0.01)
### Plot for the first arrays
i<-1
plot(Disease.FL, index=i, type="Single")
title(main=paste("Plot for the ", i ,"th BAC array", sep=""))
### Consensus plot
plot(Disease.FL, index=1:4, type="Consensus")
title(main="Consensus Plot for 4 BAC arrays")
### Plot all arrays
plot(Disease.FL, index=1:4, type="All")
title(main="Plot for all 4 arrays")
### Report and output
report<-summary(Disease.FL, index=1:4)
print(report)
output.cghFLasso(report, file="CGH.FL.output.txt")
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