Description Usage Arguments Examples
Run default erccdashboard analysis of ERCC control ratio mixtures
| 1 2 3 4 5 | 
| datType | type is "count" (RNA-Seq) or "array" (microarray), "count" is unnormalized integer count data (normalized RNA-Seq data will be accepted in an updated version of the package), "array" can be normalized or unnormalized fluorescent intensities from a microarray experiment. | 
| isNorm | default is FALSE, if FALSE then the unnormalized input data will be normalized in erccdashboard analysis. If TRUE then it is expected that the data is already normalized | 
| exTable | data frame, the first column contains names of genes or transcripts (Feature) and the remaining columns are expression measures for sample replicates spiked with ERCC controls | 
| repNormFactor | optional vector of normalization factors for each replicate, default value is NULL and 75th percentile normalization will be applied to replicates | 
| filenameRoot | string root name for output files | 
| sample1Name | string name for sample 1 in the gene expression experiment | 
| sample2Name | string name for sample 2 in the gene expression experiment | 
| erccmix | Name of ERCC mixture design, "RatioPair" is default, the other option is "Single" | 
| erccdilution | unitless dilution factor used in dilution of the Ambion ERCC spike-in mixture solutions | 
| spikeVol | volume in microliters of diluted ERCC mix spiked into the total RNA samples | 
| totalRNAmass | mass in micrograms of total RNA spiked with diluted ERCC mixtures | 
| choseFDR | False Discovery Rate for differential expression testing | 
| ratioLim | Limits for ratio axis on MA plot, default is c(-4,4) | 
| signalLim | Limits for ratio axis on MA plot, default is c(-14,14) | 
| userMixFile | optional filename input, default is NULL, if ERCC control ratio mixtures other than the Ambion product were used then a userMixFile can be used for the analysis | 
| 1 2 3 4 5 6 7 8 9 10 | data(SEQC.Example)
     
exDat = runDashboard(datType = "count",isNorm = FALSE,
                     exTable = MET.CTL.countDat, 
                     filenameRoot = "COH.ILM",
                     sample1Name = "MET", sample2Name = "CTL", 
                     erccmix = "RatioPair", erccdilution = 1/100, 
                     spikeVol = 1, totalRNAmass = 0.500,choseFDR = 0.1)
                 
summary(exDat)
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