countToFPKM (version 1.0)

fpkmheatmap: countToFPKM A FPKM heatmap plot of the highly variable features in RNA-Seq dataset

Description

fpkmheatmap() function returns a heatmap plot of the highly variable features in RNA-Seq dataset.

Usage

fpkmheatmap(fpkm_matrix, topvar=30, showfeaturenames=TRUE, return_log = TRUE)

Arguments

fpkm_matrix

A data matrix normalized by library size and feature length.

topvar

Number of highly variable features to show in heatmap plot.

showfeaturenames

whether to show the name of features in heatmap plot. The default value is TRUE.

return_log

whether to use log10 transformation of (fpkm+1). The default value is TRUE.

Value

A FPKM heatmap plot of the highly variable features in RNA-Seq dataset.

Details

The fpkmheatmap() function provides the user with a quick and reliable way to generate FPKM heatmap plot of the highly variable features in RNA-Seq dataset. It takes an FPKM numeric matrix which can be obtained using the fpkm() function as input. By default using Pearson correlation - 1 to measure the distance between features, and Spearman correlation -1 for clustering of samples. By default log10 transformation of (FPKM+1) is applied to make variation similar across orders of magnitude. It then uses the var() function to identify the highly variable features to create the heatmap plot using the Heatmap() function from the 'ComplexHeatmap' package.

References

Trapnell,C. et al. (2010) Transcript assembly and quantification by RNA-seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat. Biotechnol., 28, 511-515. doi: 10.1038/nbt.1621.

Examples

# NOT RUN {
library(countToFPKM)

file.readcounts <- system.file("extdata", "RNA-seq.read.counts.csv", package="countToFPKM")
file.annotations <- system.file("extdata", "Biomart.annotations.hg38.txt", package="countToFPKM")
file.sample.metrics <- system.file("extdata", "RNA-seq.samples.metrics.txt", package="countToFPKM")


# Import the read count matrix data into R.
counts <- as.matrix(read.csv(file.readcounts))

# Import feature annotations. 
# Assign feature length into a numeric vector.
gene.annotations <- read.table(file.annotations, sep="\t", header=TRUE)
featureLength <- gene.annotations$length

# Import sample metrics. 
# Assign mean fragment length into a numeric vector.
samples.metrics <- read.table(file.sample.metrics, sep="\t", header=TRUE)
meanFragmentLength <- samples.metrics$meanFragmentLength

# Return FPKM into a numeric matrix.
fpkm_matrix <- fpkm (counts, featureLength, meanFragmentLength)

# Plot log10(FPKM+1) heatmap of top 30 highly variable features
fpkmheatmap(fpkm_matrix, topvar=30, showfeaturenames=TRUE, return_log = TRUE)
# }