normaliseCountMatrix,scRNAseq-method {conclus} | R Documentation

## normaliseCountMatrix

### Description

This function uses coldata (cells informations) and rowdata (genes informations) to filter the count matrix. It also normalizes by using deconvolution with size factors.

### Usage

    normaliseCountMatrix(theObject, sizes=c(20,40,60,80,100), rowdata=NULL,
                        coldata=NULL, alreadyCellFiltered=FALSE,
                        runQuickCluster=TRUE, info=TRUE, removeNoSymbol=FALSE)

### Arguments

`theObject` | A scRNAseq object
`sizes` | Vector of size factors used by scran::computeSumFactors(). It is a numeric vector of pool sizes, i.e., number of cells per pool. See ?scran::computeSumFactors for more details.
`rowdata` | Data frame containing genes informations. Default is NULL.
`coldata` | Data frame containing cells informations. Default is NULL.
`alreadyCellFiltered` | Logical. If TRUE, quality check and filtering will not be applied.
`runQuickCluster` | Logical. If TRUE scran::quickCluster() function will be applied. It usually improves the normalization for medium-size count matrices. However, it is not recommended for datasets with less than 200 cells and may take too long for datasets with more than 10000 cells.
`info` | Logical. If TRUE, additional annotations like ensembl_gene_id, go_id, name_1006, chromosome_name and gene_biotype are added to the row data, for all the genes from the count matrix with ENSEMBL IDs or SYMBOL ID. Default: TRUE.
`removeNoSymbol` | Logical. If TRUE, genes with no SYMBOL are removed after the normalization

### Details

This function uses the normalization method of the scater package. For more details about the normalization used see ?scater::normalize. The size factors used in the normalization are calculated with scran::computeSumFactors.

Beforehand, the function will annotate genes creating rowData and add statistics about cells into columnsMetaData. If you already have columnsMetaData and rowData, you can give it to the function (see manual). It will keep your columns and add new ones at the end. If you do not want to lose any cell after quality metrics check, select alreadyCellFiltered = TRUE, by default it is FALSE. Before scater normalization, the function will call scran::quickCluster (see manual for details). If you want to skip this step, set runQuickCluster = FALSE, by default it is TRUE. We advice to first try the analysis with this option and to set it to FALSE if no rare populations are found.

### Value

Returns a scRNASeq object with its sceNorm slot updated. This slot contains a SingleCellExperiment object having the normalized count matrix, the colData (table with cells informations), and the rowData (table with the genes informations). See ?SingleCellExperiment for more details.

### Author(s)

Ilyess RACHEDI, based on code by Polina PAVLOVICH and Nicolas DESCOSTES.

### Examples

    ## Load the count matrix
    countmatrixPath <- system.file("extdata/countMatrix.tsv", package="conclus")
    countMatrix <- loadDataOrMatrix(file=countmatrixPath, type="countMatrix",
                                    ignoreCellNumber=TRUE)

    ## Load the coldata
    coldataPath <- system.file("extdata/colData.tsv", package="conclus")
    columnsMetaData <- loadDataOrMatrix(file=coldataPath, type="coldata",
    columnID="cell_ID")

    ## Create the initial object
    scr <- singlecellRNAseq(experimentName = "Bergiers",
                    countMatrix     = countMatrix,
                    species         = "mouse",
                    outputDirectory = "YourOutputDirectory")

    ## Normalize and filter the raw counts matrix
    scr <- normaliseCountMatrix(scr, coldata = columnsMetaData, info=FALSE)

[Package conclus version 1.2.4 Index]