kCluster {clusterSeq} | R Documentation

## Constructs co-expression dissimilarities from k-means analyses.

### Description

This function aims to find pairwise distances between genes. It does this by constructing k-means clusterings of the observed (log) expression for each gene, and for each pair of genes, finding the maximum value of k for which the centroids of the clusters are monotonic between the genes.

### Usage

    kCluster(cD, maxK = 100, matrixFile = NULL, replicates =
      NULL, algorithm = "Lloyd", B = 1000, sdm = 1)

### Arguments

`cD` | A `countData` object containing the raw count data for each gene, or a matrix containing the logged and normalised values for each gene (rows) and sample (columns).
`maxK` | The maximum value of k for which k-means clustering will be performed. Defaults to 100.
`matrixFile` | If given, a file to write the complete (gzipped) matrix of pairwise distances between genes. Defaults to NULL.
`replicates` | If given, a factor or vector that can be cast to a factor that defines the replicate structure of the data. See Details.
`algorithm` | The algorithm to be used by the kmeans function.
`B` | Number of iterations of bootstrapping algorithm used to establish clustering validity
`sdm` | Thresholding parameter for validity; see Details.

### Details

In comparing two genes, we find the maximum value of k for which separate k-means clusterings of the two genes lead to a monotonic relationship between the centroids of the clusters. For this value of k, the maximum difference between expression levels observed within a cluster of either gene is reported as a measure of the dissimilarity between the two genes.

There is a potential issue in that for genes non-differentially expressed across all samples (i.e., the appropriate value of k is 1), there will nevertheless exist clusterings for k > 1. For some arrangements of data, this leads to misattribution of non-differentially expressed genes. We identify these cases by adapting Tibshirani's gap statistic; bootstrapping uniformly distributed data on the same range as the observed data, calculating the dissimilarity score as above, and finding those cases for which the gap between the bootstrapped mean dissimilarity and the observed dissimilarity for k = 1 exceeds that for k = 2 by more than some multiple (sdm) of the standard error of the bootstrapped dissimilarities of k = 2. These cases are forced to be treated as non-differentially expressed by discarding all dissimilarity data for k > 1.

If the replicates vector is given, or if the replicates slot of a `countData` given as the 'cD' variable is complete, then the k-means clustering will be done on the median of the expression values of each replicate group. Dissimilarity calculations will still be made on the full data.

### Value

A data.frame which for each gene defines its nearest neighbour of higher row index and the dissimilarity with that neighbour.

### Author(s)

Thomas J. Hardcastle

### See Also

`makeClusters` `makeClustersFF` `associatePosteriors`

### Examples

    #Load in the processed data of observed read counts at each gene for each sample.
    data(ratThymus, package = "clusterSeq")

    # Library scaling factors are acquired here using the getLibsizes
    # function from the baySeq package.
    libsizes <- getLibsizes(data = ratThymus)

    # Adjust the data to remove zeros and rescale by the library scaling
    # factors. Convert to log scale.
    ratThymus[ratThymus == 0] <- 1
    normRT <- log2(t(t(ratThymus / libsizes)) * mean(libsizes))

    # run kCluster on reduced set.
    normRT <- normRT[1:1000,]
    kClust <- kCluster(normRT)
    head(kClust)

    # Alternatively, run on a count data object:
    # load in analysed countData (baySeq package) object
    library(baySeq)
    data(cD.ratThymus, package = "clusterSeq")

    # estimate likelihoods of dissimilarity on reduced set
    kClust2 <- kCluster(cD.ratThymus[1:1000,])
    head(kClust2)

[Package clusterSeq version 1.18.0 Index]