Package 'iClusterPlus' reference manual

Title:	Integrative clustering of multi-type genomic data
Description:	Integrative clustering of multiple genomic data using a joint latent variable model.
Authors:	Qianxing Mo, Ronglai Shen
Maintainer:	Qianxing Mo <[email protected]>, Ronglai Shen <[email protected]>
License:	GPL (>= 2)
Version:	1.43.1
Built:	2024-11-23 03:00:16 UTC
Source:	https://github.com/bioc/iClusterPlus

Breast cancer data set DNA copy number and mRNA expression measure on chromosome 17

Description

This is a subset of the breast cancer data from Pollack et al. (2002).

Usage

data(breast.chr17)data(breast.chr17)

Format

A list object containing two data matrices: DNA and mRNA. They consist chromosome 17 data in 41 samples (4 cell lines and 37 primary tumors).

Source

This data can be downloaded at http://www.pnas.org/content/99/20/12963/suppl/DC1

References

Pollack, J.R. et al. (2002) Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors. Proc. Natl Acad. Sci. USA, 99, 12963-12968.

A function to remove redundant copy number regions

Description

This function is used to reduce copy number regions.

Usage

CNregions(seg, epsilon=0.005, adaptive=FALSE, rmCNV=FALSE, cnv=NULL,
	       frac.overlap=0.5, rmSmallseg=TRUE, nProbes=15)
CNregions(seg, epsilon=0.005, adaptive=FALSE, rmCNV=FALSE, cnv=NULL,
	       frac.overlap=0.5, rmSmallseg=TRUE, nProbes=15)

Arguments

`seg`	DNAcopy CBS segmentation output.
`epsilon`	the maximum Euclidean distance between adjacent probes tolerated for denying a nonredundant region. epsilon=0 is equivalent to taking the union of all unique break points across the n samples.
`adaptive`	Vector of length-m lasso penalty terms.
`rmCNV`	If TRUE, remove germline CNV.
`cnv`	A data frame containing germline CNV data.
`frac.overlap`	A parameter needed to be explain.
`rmSmallseg`	If TRUE, remove small segment.
`nProbes`	The segment length threshold below which the segment will be removed if rmSmallseq = TRUE.

Value

A matrix with reduced copy number regions.

Author(s)

Ronglai Shen [email protected]

References

Qianxing Mo, Sijian Wang, Venkatraman E. Seshan, Adam B. Olshen, Nikolaus Schultz, Chris Sander, R. Scott Powers, Marc Ladanyi, and Ronglai Shen. (2013). Pattern discovery and cancer gene identification in integrated cancer genomic data. Proc. Natl. Acad. Sci. USA.

Examples


#data(gbm)
#library(GenomicRanges)
#library(cluster)
#reducedM=CNregions(seg,epsilon=0,adaptive=FALSE,rmCNV=TRUE,cnv=NULL,
#  frac.overlap=0.5, rmSmallseg=TRUE,nProbes=5)

#data(gbm)
#library(GenomicRanges)
#library(cluster)
#reducedM=CNregions(seg,epsilon=0,adaptive=FALSE,rmCNV=TRUE,cnv=NULL,
#  frac.overlap=0.5, rmSmallseg=TRUE,nProbes=5)

A function to compute the proportion of deviation from perfect block diagonal matrix

Description

A function to compute the proportion of deviation from perfect block diagonal matrix.

Usage

compute.pod(fit)
compute.pod(fit)

Arguments

fit

A iCluster object

Value

pod

proportion of deviation from perfect block diagonal matrix

Author(s)

Ronglai Shen [email protected]

References

Ronglai Shen, Adam Olshen, Marc Ladanyi. (2009). Integrative clustering of multiple genomic data types using a joint latent variable model with application to breast and lung cancer subtype analysis. Bioinformatics 25, 2906-2912.

Examples

# library(iCluster)
# data(breast.chr17)
# fit=iCluster(breast.chr17, k=4, lambda=c(0.2,0.2))
# plotiCluster(fit=fit, label=rownames(breast.chr17[[2]]))
# compute.pod(fit)
# library(iCluster)
# data(breast.chr17)
# fit=iCluster(breast.chr17, k=4, lambda=c(0.2,0.2))
# plotiCluster(fit=fit, label=rownames(breast.chr17[[2]]))
# compute.pod(fit)

genomic coordinates

Description

genomic coordinates for the copy number data in gbm

Usage

data(coord)data(coord)

Format

A data matrix consists of chr number, start and end position for the genes included in the gbm copy number data.

References

Ronglai Shen, Qianxing Mo, Nikolaus Schultz, Venkatraman E. Seshan, Adam B. Olshen, Jason Huse, Marc Ladanyi, Chris Sander. (2012). Integrative Subtype Discovery in Glioblastoma Using iCluster. PLoS ONE 7, e35236

GBM data

Description

This is a subset of the glioblastoma dataset from the cancer genome atlas (TCGA) GBM study (2009) used in Shen et al. (2012).

Usage

data(gbm)data(gbm)

Format

A list object containing three data matrices: copy number, methylation and mRNA expression in 84 samples.

Value

`gbm.seg`	GBM copy number segmentation results genereated by DNAcopy package.
`gbm.exp`	GBM gene expression data.
`gbm.mut`	GBM mutation data.

References

good lattice points using the uniform design

Description

good lattice points using the uniform design (Fang and Wang 1995)

Usage

data(glp)data(glp)

Format

A list object containing sampling design for s=2-5 where s is the number of tuning parameters.

References

Fang K, Wang Y (1994) Number theoretic methods in statistics. London, UK: Chapman abd Hall.

Integrative clustering of multiple genomic data types

Description

Given multiple genomic data types (e.g., copy number, gene expression, DNA methylation) measured in the same set of samples, iCluster fits a regularized latent variable model based clustering that generates an integrated cluster assigment based on joint inference across data types

Usage

iCluster(datasets, k, lambda, scalar=FALSE, max.iter=50,epsilon=1e-3)
iCluster(datasets, k, lambda, scalar=FALSE, max.iter=50,epsilon=1e-3)

Arguments

`datasets`	A list object containing m data matrices representing m different genomic data types measured in a set of n samples. For each matrix, the rows represent samples, and the columns represent genomic features.
`k`	Number of subtypes.
`lambda`	Vector of length-m lasso penalty terms.
`scalar`	If TRUE, assumes scalar covariance matrix Psi. Default is FALSE.
`max.iter`	Maximum iteration for the EM algorithm.
`epsilon`	EM algorithm convegence criterion.

Value

A list with the following elements.

`meanZ`	Relaxed cluster indicator matrix.
`beta`	Coefficient matrix.
`clusters`	Cluster assigment.
`conv.rate`	Convergence history.

Author(s)

Ronglai Shen [email protected]

References

Examples


data(breast.chr17)
fit=iCluster(breast.chr17, k=4, lambda=c(0.2,0.2))
plotiCluster(fit=fit, label=rownames(breast.chr17[[2]]))
compute.pod(fit)

#library(gplots)
#library(lattice)
#col.scheme = alist()
#col.scheme[[1]] = bluered(256)
#col.scheme[[2]] = greenred(256)
#cn.image=breast.chr17[[2]]
#cn.image[cn.image>1.5]=1.5
#cn.image[cn.image< -1.5]= -1.5
#exp.image=breast.chr17[[1]]
#exp.image[exp.image>3]=3
#exp.image[exp.image< -3]=3
#plotHeatmap(fit, datasets=list(cn.image,exp.image), type=c("gaussian","gaussian"),
#  row.order=c(FALSE,FALSE), width=5, col.scheme=col.scheme)
data(breast.chr17)
fit=iCluster(breast.chr17, k=4, lambda=c(0.2,0.2))
plotiCluster(fit=fit, label=rownames(breast.chr17[[2]]))
compute.pod(fit)

#library(gplots)
#library(lattice)
#col.scheme = alist()
#col.scheme[[1]] = bluered(256)
#col.scheme[[2]] = greenred(256)
#cn.image=breast.chr17[[2]]
#cn.image[cn.image>1.5]=1.5
#cn.image[cn.image< -1.5]= -1.5
#exp.image=breast.chr17[[1]]
#exp.image[exp.image>3]=3
#exp.image[exp.image< -3]=3
#plotHeatmap(fit, datasets=list(cn.image,exp.image), type=c("gaussian","gaussian"),
#  row.order=c(FALSE,FALSE), width=5, col.scheme=col.scheme)

Integrative clustering of multiple genomic data types

Description

Usage

iCluster2(x, K, lambda, method=c("lasso","enet","flasso","glasso","gflasso"),
  chr=NULL, maxiter=50, eps=1e-4, eps2=1e-8)
iCluster2(x, K, lambda, method=c("lasso","enet","flasso","glasso","gflasso"),
  chr=NULL, maxiter=50, eps=1e-4, eps2=1e-8)

Arguments

`x`	A list object containing m data matrices representing m different genomic data types measured in a set of n samples. For each matrix, the rows represent samples, and the columns represent genomic features.
`K`	Number of subtypes.
`lambda`	A list with m elements; each element is a vector with one or two elements depending on the methods used.
`method`	Method used for clustering and variable selection.
`chr`	Chromosome labels
`maxiter`	Maximum iteration for the EM algorithm.
`eps`	EM algorithm convegence criterion 1.
`eps2`	EM algorithm convegence criterion 2.

Value

A list with the following elements.

`cluster`	Cluster assigment.
`centers`	cluster centers.
`Phivec`	parameter phi; a vector.
`beta`	parameter B; a matrix.
`meanZ`	meanZ
`EZZt`	EZZt
`dif`	difference
`iter`	iteration

Author(s)

Qianxing Mo [email protected],Ronglai Shen,Sijian Wang

References

Ronglai Shen, Sijian Wang, Qianxing Mo. (2013). Sparse Integrative Clustering of Multiple Omics Data Sets. Annals of Applied Statistics. 7(1):269-294

Examples


## clustering
n1 = 20
n2 = 20
n3 = 20
n = n1+n2+n3
p = 5
q = 100

x = NULL
x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[1]] = cbind(xa,xb)

x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[2]] = cbind(xa,xb)

x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[3]] = cbind(xa,xb)


x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[4]] = cbind(xa,xb)

x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[5]] = cbind(xa,xb)

method = c('lasso', 'enet', 'flasso', 'glasso', 'gflasso')  
lambda=alist()
lambda[[1]] = 30
lambda[[2]] = c(20,1)
lambda[[3]] = c(20,20)
lambda[[4]] = 30
lambda[[5]] = c(30,20)

chr=c(rep(1,10),rep(2,(p+q)-10)) 
date()
fit2 = iCluster2(x, K=3, lambda, method=method, chr=chr, maxiter=20,eps=1e-4, eps2=1e-8)
date()

par(mfrow=c(5,1),mar=c(4,4,1,1))
for(i in 1:5){
barplot(fit2$beta[[i]][,1])
}

#library(gplots)
#library(lattice)

#plotHeatmap(fit2, datasets=x, type=rep("gaussian",length(x)),
   #row.order=c(TRUE,TRUE,FALSE,TRUE,FALSE), 
   #sparse=rep(FALSE,length(x)), scale=rep("row",5), width=5,
   #col.scheme=rep(list(bluered(256)),length(x)))

## clustering
n1 = 20
n2 = 20
n3 = 20
n = n1+n2+n3
p = 5
q = 100

x = NULL
x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[1]] = cbind(xa,xb)

x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[2]] = cbind(xa,xb)

x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[3]] = cbind(xa,xb)


x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[4]] = cbind(xa,xb)

x1a = matrix(rnorm(n1*p), ncol=p)
x2a = matrix(rnorm(n1*p, -1.5,1), ncol=p)
x3a = matrix(rnorm(n1*p, 1.5, 1), ncol=p)
xa = rbind(x1a,x2a,x3a)
xb = matrix(rnorm(n*q), ncol=q)
x[[5]] = cbind(xa,xb)

method = c('lasso', 'enet', 'flasso', 'glasso', 'gflasso')  
lambda=alist()
lambda[[1]] = 30
lambda[[2]] = c(20,1)
lambda[[3]] = c(20,20)
lambda[[4]] = 30
lambda[[5]] = c(30,20)

chr=c(rep(1,10),rep(2,(p+q)-10)) 
date()
fit2 = iCluster2(x, K=3, lambda, method=method, chr=chr, maxiter=20,eps=1e-4, eps2=1e-8)
date()

par(mfrow=c(5,1),mar=c(4,4,1,1))
for(i in 1:5){
barplot(fit2$beta[[i]][,1])
}

#library(gplots)
#library(lattice)

#plotHeatmap(fit2, datasets=x, type=rep("gaussian",length(x)),
   #row.order=c(TRUE,TRUE,FALSE,TRUE,FALSE), 
   #sparse=rep(FALSE,length(x)), scale=rep("row",5), width=5,
   #col.scheme=rep(list(bluered(256)),length(x)))

Integrative clustering of multiple genomic data types

Description

Given multiple genomic data types (e.g., copy number, gene expression, DNA methylation) measured in the same set of samples, iClusterBayes fits a Bayesian latent variable model that generates an integrated cluster assignment based on joint inference across data types and identifies genomic features that contribute to the clusters.

Usage

iClusterBayes(dt1,dt2=NULL,dt3=NULL,dt4=NULL,dt5=NULL,dt6=NULL,
	type = c("gaussian","binomial","poisson"),K=2,n.burnin=1000,n.draw=1200,
	prior.gamma=rep(0.1,6),sdev=0.5,beta.var.scale=1,thin=1,pp.cutoff=0.5)
iClusterBayes(dt1,dt2=NULL,dt3=NULL,dt4=NULL,dt5=NULL,dt6=NULL,
	type = c("gaussian","binomial","poisson"),K=2,n.burnin=1000,n.draw=1200,
	prior.gamma=rep(0.1,6),sdev=0.5,beta.var.scale=1,thin=1,pp.cutoff=0.5)

Arguments

`dt1`	Data set 1 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt2`	Data set 2 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt3`	Data set 3 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt4`	Data set 4 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt5`	Data set 5 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt6`	Data set 6 - a matrix with rows and columns representing samples and genomic features, respectively.
`type`	Data type corresponding to dt1-6, which can be gaussian, binomial, or poisson.
`K`	The number of eigen features. Given K, the number of cluster is K+1.
`n.burnin`	Number of MCMC burnin.
`n.draw`	Number of MCMC draw.
`prior.gamma`	Prior probability for the indicator variable gamma of each data set.
`sdev`	Standard deviation of random walk proposal for the latent variable.
`beta.var.scale`	A positive value to control the scale of covariance matrix of the proposed beta.
`thin`	A parameter to thin the MCMC chain in order to reduce autocorrelation. Discard all but every 'thin'th sampling values. When thin=1, all sampling values are kept.
`pp.cutoff`	Posterior probability cutoff for the indicator variable gamma. The BIC and deviance ratio will be calculated by setting parameter beta to zero when the posterior probability of gamma <= cutoff.

Value

A list with the following elements.

`alpha`	Intercept parameter.
`beta`	Information parameter.
`beta.pp`	Posterior probability of beta. The higher the beta.pp, the more likely the beta should be included in the model.
`gamma.ar`	Acceptance ratio for the parameter gamma.
`beta.ar`	Acceptance ratio for the parameter beta.
`Z.ar`	Acceptance ratio for the latent variable.
`clusters`	Cluster assignment.
`centers`	Cluster center.
`meanZ`	The latent variable.
`BIC`	Bayesian information criterion.
`dev.ratio`	see dev.ratio defined in glmnet package.

Author(s)

Qianxing Mo [email protected]

References

Mo Q, Shen R, Guo C, Vannucci M, Chan KS, Hilsenbeck SG. (2018). A fully Bayesian latent variable model for integrative clustering analysis of multi-type omics data. Biostatistics 19(1):71-86.

Examples

# see iManual.pdf
# see iManual.pdf

Integrative clustering of multiple genomic data types

Description

Given multiple genomic data types (e.g., copy number, gene expression, DNA methylation) measured in the same set of samples, iClusterPlus fits a regularized latent variable model based clustering that generates an integrated cluster assignment based on joint inference across data types

Usage

iClusterPlus(dt1,dt2=NULL,dt3=NULL,dt4=NULL,
	type=c("gaussian","binomial","poisson","multinomial"),
 	K=2,alpha=c(1,1,1,1),lambda=c(0.03,0.03,0.03,0.03),
	n.burnin=100,n.draw=200,maxiter=20,sdev=0.05,eps=1.0e-4)
iClusterPlus(dt1,dt2=NULL,dt3=NULL,dt4=NULL,
	type=c("gaussian","binomial","poisson","multinomial"),
 	K=2,alpha=c(1,1,1,1),lambda=c(0.03,0.03,0.03,0.03),
	n.burnin=100,n.draw=200,maxiter=20,sdev=0.05,eps=1.0e-4)

Arguments

`dt1`	A data matrix. The rows represent samples, and the columns represent genomic features.
`dt2`	A data matrix. The rows represent samples, and the columns represent genomic features.
`dt3`	A data matrix. The rows represent samples, and the columns represent genomic features.
`dt4`	A data matrix. The rows represent samples, and the columns represent genomic features.
`type`	Data type, which can be gaussian, binomial, poisson, multinomial.
`K`	The number of eigen features. Given K, the number of cluster is K+1.
`alpha`	Vector of elasticnet penalty terms. At this version of iClusterPlus, elasticnet is not used. Therefore, all the elements of alpha are set to 1.
`lambda`	Vector of lasso penalty terms.
`n.burnin`	Number of MCMC burnin.
`n.draw`	Number of MCMC draw.
`maxiter`	Maximum iteration for the EM algorithm.
`sdev`	standard deviation of random walk proposal.
`eps`	Algorithm convergence criterion.

Value

A list with the following elements.

`alpha`	Intercept parameter.
`beta`	Information parameter.
`clusters`	Cluster assignment.
`centers`	Cluster center.
`meanZ`	Latent variable.
`BIC`	Bayesian information criterion.
`dev.ratio`	see dev.ratio defined in glmnet package.
`dif`	absolute difference for the parameters in the last and next-to-last iterations.

Author(s)

Qianxing Mo [email protected],Ronglai Shen, Sijian Wang

References

Examples

# see iManual.pdf
# see iManual.pdf

A function to generate heatmap panels sorted by integrated cluster assignment.

Description

A function to generate heatmap panels sorted by integrated cluster assignment.

Usage

plotHeatmap(fit,datasets,type=c("gaussian","binomial","poisson","multinomial"),
	sample.order=NULL,row.order=NULL,sparse=NULL,threshold=rep(0.25,length(datasets)),
	width=5,scale=rep("none",length(datasets)),col.scheme=rep(list(bluered(256)),
	length(datasets)), chr=NULL, plot.chr=NULL, cap=NULL)
plotHeatmap(fit,datasets,type=c("gaussian","binomial","poisson","multinomial"),
	sample.order=NULL,row.order=NULL,sparse=NULL,threshold=rep(0.25,length(datasets)),
	width=5,scale=rep("none",length(datasets)),col.scheme=rep(list(bluered(256)),
	length(datasets)), chr=NULL, plot.chr=NULL, cap=NULL)

Arguments

`fit`	A iCluster object.
`datasets`	A list object of data matrices.
`type`	Types of data in the datasets.
`sample.order`	User supplied cluster assignment.
`row.order`	A vector of logical values each specificy whether the genomic features in the corresponding data matrix should be reordered by similarity. Default is TRUE.
`sparse`	A vector of logical values each specificy whether to plot the top cluster-discriminant features. Default is FALSE.
`threshold`	When sparse is TRUE, a vector of threshold values to include the genomic features for which the absolute value of the associated coefficient estimates fall in the top quantile. threshold=c(0.25,0.25) takes the top quartile most discriminant features in data type 1 and data type 2 for plot.
`width`	Width of the figure in inches
`scale`	A vector of logical values each specify whether data should be scaled. Default is FALSE.
`col.scheme`	Color scheme. Can use bluered(n) in gplots R package.
`chr`	A vector of chromosome number.
`plot.chr`	A vector of logical values each specificy whether to annotate chromosome number on the left of the panel. Typically used for copy number data type. Default is FALSE.
`cap`	Image color option

Details

The samples are ordered by the cluster assignment using the R code: order(fit$clusters). For each data set, the features are ordered by hierarchical clustering of the features using the complete method and 1-correlation coeffient as the distance.

Value

no value returned.

Author(s)

Ronglai Shen [email protected]

References

Examples

# see iManual.pdf
# see iManual.pdf

A function to generate heatmap panels sorted by integrated cluster assignment.

Description

A function to generate heatmap panels sorted by integrated cluster assignment.

Usage

plotHMBayes(fit, datasets, type = c("gaussian", "binomial", "poisson"),
    sample.order = NULL, row.order = NULL, sparse = NULL, 
    threshold = rep(0.5,length(datasets)), width = 5,
    scale = rep("none",length(datasets)), 
    col.scheme = rep(list(bluered(256)),length(datasets)),
    chr=NULL, plot.chr=NULL, cap=NULL)
plotHMBayes(fit, datasets, type = c("gaussian", "binomial", "poisson"),
    sample.order = NULL, row.order = NULL, sparse = NULL, 
    threshold = rep(0.5,length(datasets)), width = 5,
    scale = rep("none",length(datasets)), 
    col.scheme = rep(list(bluered(256)),length(datasets)),
    chr=NULL, plot.chr=NULL, cap=NULL)

Arguments

`fit`	A iClusterBayes object.
`datasets`	A list object of data matrices.
`type`	Types of data in the datasets.
`sample.order`	User supplied cluster assignment.
`row.order`	A vector of logical values each specify whether the genomic features in the corresponding data matrix should be reordered by similarity. Default is TRUE.
`sparse`	A vector of logical values each specify whether to plot the top cluster-discriminant features. Default is FALSE.
`threshold`	When sparse is TRUE, a vector of threshold values to include the genomic features on the heatmap. Each data set should have a threshold. For each data set, a feature with posterior probability greater than the threshold will be included. Default value is 0.5 for each data set.
`width`	Width of the figure in inches
`scale`	A vector of logical values each specify whether data should be scaled. Default is FALSE.
`col.scheme`	Color scheme. Can use bluered(n) in gplots R package.
`chr`	A vector of chromosome number.
`plot.chr`	A vector of logical values each specify whether to annotate chromosome number on the left of the panel. Typically used for copy number data type. Default is FALSE.
`cap`	Image color option

Details

The samples are ordered by the cluster assignment by the R code: order(fit$clusters). For each data set, the features are ordered by hierarchical clustering of the features using the complete method and 1-correlation coefficient as the distance.

Value

no value returned.

Author(s)

Ronglai Shen [email protected],Qianxing Mo [email protected]

References

Mo Q, Shen R, Guo C, Vannucci M, Chan KS, Hilsenbeck SG. (2018). A fully Bayesian latent variable model for integrative clustering analysis of multi-type omics data. Biostatistics 19(1):71-86.

Examples

# see iManual.pdf
# see iManual.pdf

A function to generate cluster separability matrix plot.

Description

A function to generate cluster separability matrix plot.

Usage

plotiCluster(fit,label=NULL)
plotiCluster(fit,label=NULL)

Arguments

`fit`	A iCluster object
`label`	Sample labels

Value

no value returned.

Author(s)

Ronglai Shen [email protected]

References

Examples

# library(iCluster)
# data(breast.chr17)
# fit=iCluster(datasets=breast.chr17, k=4, lambda=c(0.2,0.2))
# plotiCluster(fit=fit, label=rownames(breast.chr17[[2]]))
# compute.pod(fit)
# library(iCluster)
# data(breast.chr17)
# fit=iCluster(datasets=breast.chr17, k=4, lambda=c(0.2,0.2))
# plotiCluster(fit=fit, label=rownames(breast.chr17[[2]]))
# compute.pod(fit)

A function to generate reproducibility index plot.

Description

A function to generate reproducibility index plot.

Usage

plotRI(cv.fit)
plotRI(cv.fit)

Arguments

cv.fit

A tune.iCluster2 object

Value

no value returned.

Author(s)

Ronglai Shen [email protected]

References

Examples

#data(simu.datasets)
#cv.fit=alist()
#for(k in 2:5){
#  cat(paste("K=",k,sep=""),'\n')
#  cv.fit[[k]]=tune.iCluster2(datasets=simu.datasets, k,nrep=2, n.lambda=8)
#}

##Reproducibility index (RI) plot
#plotRI(cv.fit)
#data(simu.datasets)
#cv.fit=alist()
#for(k in 2:5){
#  cat(paste("K=",k,sep=""),'\n')
#  cv.fit[[k]]=tune.iCluster2(datasets=simu.datasets, k,nrep=2, n.lambda=8)
#}

##Reproducibility index (RI) plot
#plotRI(cv.fit)

The results for the analysis of the simulated data.

Description

The simulation and analyis are described in iClusterPlus/inst/unitTests/test_iClusterPlus.R.

Usage

data(simuResult)data(simuResult)

Format

list

Value

A list of objects returned by the iClusterPlus function.

References

iClusterPlus/inst/unitTests/test_iClusterPlus.R

Integrative clustering of multiple genomic data types

Description

Usage

tune.iCluster2(x, K, method=c("lasso","enet","flasso","glasso","gflasso"),base=200,
  chr=NULL,true.class=NULL,lambda=NULL,n.lambda=NULL,save.nonsparse=F,nrep=10,eps=1e-4)
tune.iCluster2(x, K, method=c("lasso","enet","flasso","glasso","gflasso"),base=200,
  chr=NULL,true.class=NULL,lambda=NULL,n.lambda=NULL,save.nonsparse=F,nrep=10,eps=1e-4)

Arguments

`x`	A list object containing m data matrices representing m different genomic data types measured in a set of n samples. For each matrix, the rows represent samples, and the columns represent genomic features.
`K`	Number of subtypes.
`lambda`	User supplied matrix of lambda to tune.
`method`	Method used for clustering and variable selection.
`chr`	Chromosome labels
`n.lambda`	Number of lambda to sample using uniform design.
`nrep`	Fold of cross-validation.
`base`	Base.
`true.class`	True class label if available.
`save.nonsparse`	Logic argument whether to save the nonsparse fit.
`eps`	EM algorithm convergence criterion

Value

A list with the following elements.

`best.fit`	Best fit.
`best.lambda`	Best lambda.
`ps`	Rand index
`ps.adjusted`	Adjusted Rand index.

Author(s)

Qianxing Mo [email protected],Ronglai Shen,Sijian Wang

References

Ronglai Shen, Sijian Wang, Qianxing Mo. (2013). Sparse Integrative Clustering of Multiple Omics Data Sets. Annals of Applied Statistics. 7(1):269-294

Integrative clustering of multiple genomic data

Description

In order to determining the appropriate number of clusters, tune.iClusterBayes calls iClusterBayes function and performs parallel computation for K=1,2,....

Usage

tune.iClusterBayes(cpus=6,dt1,dt2=NULL,dt3=NULL,dt4=NULL,dt5=NULL,dt6=NULL,
	type=c("gaussian","binomial","poisson"),
   	K=1:6,n.burnin=1000,n.draw=1200,prior.gamma=rep(0.1,6),
	sdev=0.5,beta.var.scale=1,thin=1,pp.cutoff=0.5)
tune.iClusterBayes(cpus=6,dt1,dt2=NULL,dt3=NULL,dt4=NULL,dt5=NULL,dt6=NULL,
	type=c("gaussian","binomial","poisson"),
   	K=1:6,n.burnin=1000,n.draw=1200,prior.gamma=rep(0.1,6),
	sdev=0.5,beta.var.scale=1,thin=1,pp.cutoff=0.5)

Arguments

`cpus`	Number of CPU used for parallel computation. If possible, let it be equal to the number of Ks.
`dt1`	Data set 1 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt2`	Data set 2 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt3`	Data set 3 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt4`	Data set 4 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt5`	Data set 5 - a matrix with rows and columns representing samples and genomic features, respectively.
`dt6`	Data set 6 - a matrix with rows and columns representing samples and genomic features, respectively.
`type`	Data type corresponding to dt1-6, which can be gaussian, binomial, poisson.
`K`	A vector. Each element is the number of eigen features. Given k, the number of cluster is k+1.
`n.burnin`	Number of MCMC burnin.
`n.draw`	Number of MCMC draw.
`prior.gamma`	Prior probability for the indicator variable gamma of each data set.
`sdev`	Standard deviation of random walk proposal for the latent variable.
`beta.var.scale`	A positive value to control the scale of covariance matrix of the proposed beta.
`thin`	A parameter to thin the MCMC chain in order to reduce autocorrelation. Discard all but every 'thin'th sampling values. When thin=1, all sampling values are kept.
`pp.cutoff`	Posterior probability cutoff for the indicator variable gamma. The BIC and deviance ratio will be calculated by setting parameter beta to zero when the posterior probability of gamma <= cutoff.

Value

A list named 'fit'. fit[[i]] is an object return by iClusterBayes, corresponding to the ith element in K. Each component of fit has the following elements.

`alpha`	Intercept parameter.
`beta`	Information parameter.
`beta.pp`	Posterior probability of beta. The higher the beta.pp, the more likely the beta should be included in the model.
`gamma.ar`	Acceptance ratio for parameter gamma.
`beta.ar`	Acceptance ratio for parameter beta.
`Z.ar`	Acceptance ratio for the latent variable.
`clusters`	Cluster assignment.
`centers`	Cluster center.
`meanZ`	Latent variable.
`BIC`	Bayesian information criterion.
`dev.ratio`	See dev.ratio defined in glmnet package.

Author(s)

Qianxing Mo [email protected]

References

Mo Q, Shen R, Guo C, Vannucci M, Chan KS, Hilsenbeck SG. (2018). A fully Bayesian latent variable model for integrative clustering analysis of multi-type omics data. Biostatistics 19(1):71-86.

Examples

### see the users' guide iManul.pdf 
### see the users' guide iManul.pdf

Integrative clustering of multiple genomic data

Description

Given multiple genomic data (e.g., copy number, gene expression, DNA methylation) measured in the same set of samples, tune.iClusterPlus uses a series of lambda values to fit a regularized latent variable model based clustering that generates an integrated cluster assignment based on joint inference across data.

Usage

tune.iClusterPlus(cpus=8,dt1,dt2=NULL,dt3=NULL,dt4=NULL,
  type=c("gaussian","binomial","poisson","multinomial"),
  K=2,alpha=c(1,1,1,1),n.lambda=NULL,scale.lambda=c(1,1,1,1),
  n.burnin=200,n.draw=200,maxiter=20,sdev=0.05,eps=1.0e-4)
tune.iClusterPlus(cpus=8,dt1,dt2=NULL,dt3=NULL,dt4=NULL,
  type=c("gaussian","binomial","poisson","multinomial"),
  K=2,alpha=c(1,1,1,1),n.lambda=NULL,scale.lambda=c(1,1,1,1),
  n.burnin=200,n.draw=200,maxiter=20,sdev=0.05,eps=1.0e-4)

Arguments

`cpus`	Number of CPU used for parallel computation.
`dt1`	A data matrix. The rows represent samples, and the columns represent genomic features.
`dt2`	A data matrix. The rows represent samples, and the columns represent genomic features.
`dt3`	A data matrix. The rows represent samples, and the columns represent genomic features.
`dt4`	A data matrix. The rows represent samples, and the columns represent genomic features.
`type`	data type, which can be "gaussian","binomial","poisson", and"multinomial".
`K`	The number of eigen features. Given K, the number of cluster is K+1.
`alpha`	Vector of elasticnet penalty terms. At this version of iClusterPlus, elasticnet is not used. Therefore, all the elements of alpha are set to 1.
`n.lambda`	Number of lambda are tuned.
`scale.lambda`	A value between (0,1); the actual lambda values will be scale.lambda multiplying the lambda values of the uniform design.
`n.burnin`	Number of MCMC burnin.
`n.draw`	Number of MCMC draw.
`maxiter`	Maximum iteration for the EM algorithm.
`sdev`	standard deviation of random walk proposal.
`eps`	EM algorithm convergence criterion.

Value

A list with the two elements 'fit' and 'lambda', where fit itself is a list and lambda is a matrix. Each row of lambda is the lambda values used to fit iClusterPlus model. Each component of fit is an object return by iClusterPlus, one-to-one corresponding to the row of lambda. Each component of fit has the following objects.

`alpha`	Intercept parameter for the genomic features.
`beta`	Information parameter for the genomic features. The rows and the columns represent the genomic features and the coefficients for the latent variable, respectively.
`clusters`	Cluster assignment.
`centers`	Cluster centers.
`meanZ`	Latent variable.

Author(s)

Qianxing Mo [email protected], Ronglai Shen [email protected]

References

Qianxing Mo, Sijian Wang, Venkatraman E. Seshan, Adam B. Olshen, Nikolaus Schultz, Chris Sander, R. Scott Powers, Marc Ladanyi, and Ronglai Shen. (2012). Pattern discovery and cancer gene identification in integrated cancer genomic data. Proc. Natl. Acad. Sci. USA 110(11):4245-50.

Examples

### see the users' guide iManul.pdf 
### see the users' guide iManul.pdf

Utility functions for iClusterPlus package

Description

Some utility functions for processing the results produced by iClusterPlus methods.

Usage

getBIC(resultList)
getDevR(resultList)
getClusters(resultList)
iManual(view=TRUE)
getBIC(resultList)
getDevR(resultList)
getClusters(resultList)
iManual(view=TRUE)

Arguments

`resultList`	A list object as shown in the following example.
`view`	A logical value TRUE or FALSE

Value

`getBIC`	produce a matrix containing the BIC value for each lambda and K; the rows correspond to the lambda (vector) and the columns correspond to the K latent variables.
`getDevR`	produce a matrix containing the deviance ratio for each lambda and K; the rows correspond to the lambda (vector) and the columns correspond to the K latent variables.
`getClusters`	produce a matrix containing the cluster assigments for the samples under each K; the rows correspond to the samples; the columns correspond to the K latent variables.
`iManual`	Open the iClusterPlus User's Guide.

Author(s)

Qianxing Mo [email protected]

References

Examples

### see the users' guide iManual.pdf 

#data(simuResult)
#BIC = getBIC(simuResult)
#devR = getDevR(simuResult)
#clusters = getClusters(simuResult)
### see the users' guide iManual.pdf 

#data(simuResult)
#BIC = getBIC(simuResult)
#devR = getDevR(simuResult)
#clusters = getClusters(simuResult)

Human genome variants of the NCBI 36 (hg18) assembly

Description

Human genome variants of the NCBI 36 (hg18) assembly

Usage

data(variation.hg18.v10.nov.2010)data(variation.hg18.v10.nov.2010)

Format

data frame

Value

variation.hg18.v10.nov.2010

Human genome variants of the NCBI 36 (hg18) assembly

References

http://projects.tcag.ca/variation/tableview.asp?table=DGV_Content_Summary.txt

Package 'iClusterPlus'

Help Index

Breast cancer data set DNA copy number and mRNA expression measure on chromosome 17

Description

Usage

Format

Source

References

A function to remove redundant copy number regions

Description

Usage

Arguments

Value

Author(s)

References

See Also

Examples

A function to compute the proportion of deviation from perfect block diagonal matrix

Description

Usage

Arguments

Value

Author(s)

References

See Also

Examples

genomic coordinates

Description

Usage

Format

References

GBM data

Description

Usage

Format

Value

References

good lattice points using the uniform design

Description

Usage

Format

References

Integrative clustering of multiple genomic data types

Description

Usage

Arguments

Value

Author(s)

References

See Also

Examples

Integrative clustering of multiple genomic data types

Description

Usage

Arguments

Value

Author(s)

References

See Also

Examples

Integrative clustering of multiple genomic data types

Description

Usage

Arguments

Value

Author(s)

References

See Also

Examples

Integrative clustering of multiple genomic data types

Description

Usage

Arguments

Value

Author(s)

References

See Also

Examples

A function to generate heatmap panels sorted by integrated cluster assignment.

Description