Description Usage Arguments Details Value Author(s) References See Also Examples
This ensemble method combined four current methods (DESeq2, EBSeq, SAMSeq, NOISeq) with equal weight on their resulting FDR-adjusted P-values to identify significantly differentially expressed genes from RNA-Seq data.
1 | Combined_method(RNAseqcount, label, alpha)
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RNAseqcount |
The input RNA-Seq count matrix with rows and columns denoting features and samples, respectively. The first column of the matrix denotes names of features. |
label |
A vector for group notation such as 1s denote treatment group and 0s denote control group |
alpha |
The signifiance level |
The Combined method combined the analysis results from four current popular RNA-Seq differential analysis methods (DESeq2, EBSeq, SAMSeq, NOISeq) and declare a gene is significantly differentially expressed only when the gene is identified by all four methods.
Combined_method produces a named list with the following components:
DESeq2.sig |
Feature names identified by DESeq2 differential analysis method |
EBSeq.sig |
Feature names identified by EBSeq differential analysis method |
SAMSeq.sig |
Feature names identified by SAMSeq differential analysis method |
NOISeq.sig |
Feature names identified by NOISeq differential analysis method |
Combined.sig |
Feature names identified by Combined differential analysis method |
Combined.sig.table |
Significant feature tables from combined method including original feature counts from all samples, test statistics from DESeq2 method, and adjusted P-values from DESeq2 method |
Dongmei Li
Love MI, Huber W and Anders S (2014). “Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.” Genome Biology, 15, pp. 550. doi: 10.1186/s13059-014-0550-8. Leng N and Kendziorski C (2015). EBSeq: An R package for gene and isoform differential expression analysis of RNA-seq data. R package version 1.14.0. Tarazona S, Garcia-Alcalde F, Dopazo J, Ferrer A and Conesa A (2011). “Differential expression in RNA-seq: a matter of depth.” Genome Research, 21(12), pp. 4436.
The DESeq2, EBSeq, SAMSeq, and NOISeq packages.
1 2 3 4 5 6 7 | system.file("data", package = "ComSeq")
data("Bottomly_count")
summary(Bottomly_count)
label <- c(rep(0, 10), rep(1, 11))
Result <- Combined_method(RNAseqcount = Bottomly_count, label = label, alpha = 0.05)
summary(Result)
Result
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