significantMicroRna {AgiMicroRna} | R Documentation

## Summarize Differential Expression Results

### Description

The function summarizes the results from the differential expression analysis using the different objects that are obtained after 'limma' has been used, such as the 'MArrayLM' object with the statistics and the 'TestResults' object highlighting the significant features.

### Usage

    significantMicroRna(eset, ddset, targets, fit2,
    CM, DE, DEmethod, MTestmethod, PVcut, Mcut,verbose=FALSE)

### Arguments

`eset` | ExpressionSet containing the Total Gene processed data
`ddset` | An uRNAList object containing the Total Gene proceseed data
`targets` | data.frame with the target structure
`fit2` | MArrayLM object from `eBayes` 'limma' function
`CM` | Contrast matrix
`DE` | TestResults object
`DEmethod` | method used in decideTests, only 'separate' or 'nestedF' are implemented
`MTestmethod` | method for multiple test
`PVcut` | p value threshold to declare significant features
`Mcut` | M value threshold to select within significant features
`verbose` | logical, if `TRUE` prints out output

### Details

A list containing the genes with their statistics is generated. The significant genes above the PVcut p values are also given in a html file that links the selected miRNAS to the miRBase http://microrna.sanger.ac.uk/. A MA plots indicating the differentially expressed genes are also displayed.

When multiple contrasts are done, the method for the selection of the significant genes can be either 'separated' or 'nestedF'. See decideTests in package limma limma for a detailed description on these two methods. When 'separated' is used a list with all the genes that have been analized in limma is given. The list includes de following columns:

PROBE - Probe name (one of the probes interrogating the gene) GENE - miRNA name PROBE chr\_coord - Agilent chromosomal location M - Fold change A - Mean of the intensity for that miRNA t - moderated t-statistic pval - p value of the t-statistic adj.pval - p value adjusted by 'MTestmethod' fdr.pval - p value adjusted by fdr

Some times, the user can be set 'MTestmethod = none', in this case, it might be interesting to still see the fdr value, despite of the fact that the user has decided not apply any multiple testing correction.

If the 'nestedF' is used, then two lists are provided for each contrasts. A first containing the selected significant genes, and a second list containing the rest of the genes that have been analyzed. The columns given in this case is:

PROBE - Probe name (one of the probes interrogating the gene) GENE - miRNA name PROBE chr\_coord - Agilent chromosomal location M - Fold change A - Mean of the intensity for that miRNA t - moderated t-statistic t pval - p value of the t-statistic F - F statistic (null hypothesis: Ci = Cj, for all contrasts i, j) adj.F.pval - F p value adjusted by 'MTestmethod' fdr.F.pval - F p value adjusted by fdr

The html files, both for the 'separated' and 'nestedF' method, includes only the selected as significant genes.

### Author(s)

Pedro Lopez-Romero

### References

Smyth, G. K. (2005). Limma: linear models for microarray data. In: 'Bioinformatics and Computational Biology Solutions using R and Bioconductor'. R. Gentleman, V. Carey, S. Dudoit, R. Irizarry, W. Huber (eds), Springer, New York, pages 397–420.

miRBase: the home of microRNA data http://microrna.sanger.ac.uk/

### See Also

A 'uRNAList' example containing proccesed data is in `ddPROC` and an overview of how the processed data is produced is given in `filterMicroRna`. The ExpressionSet object can be generated using `esetMicroRna` An overview of miRNA differential expression analysis is given in `basicLimma` An example of how to get the 'TestResults' object is in `getDecideTests`

### Examples

    data(targets.micro)
    data(ddPROC)
    esetPROC=esetMicroRna(ddPROC,targets.micro,makePLOT=FALSE)

    levels.treatment=levels(factor(targets.micro$Treatment))
    treatment=factor(as.character(targets.micro$Treatment),
        levels=levels.treatment)

    levels.subject=levels(factor(targets.micro$Subject))
    subject=factor(as.character(targets.micro$Subject),
        levels=levels.subject)

    design=model.matrix(~ -1 + treatment + subject  )

    CM=cbind(MSC_AvsMSC_B=c(1,-1,0,0),
              MSC_AvsMSC_C=c(1,0,-1,0))

    fit2=basicLimma(esetPROC,design,CM,verbose=TRUE)

    DE=getDecideTests(fit2,
            DEmethod="separate",
            MTestmethod="BH",
            PVcut=0.10)

    significantMicroRna(esetPROC,
    	ddPROC,
    	targets.micro,
      	fit2,
    	CM,
    	DE,
    	DEmethod="separate",
    	MTestmethod="BH",
    	PVcut=0.10,
    	Mcut=0,
    	verbose=TRUE)

[Package AgiMicroRna version 2.38.0 Index]