construct.utr.model: Assemble a gene model based on 3' UTR counts for quant-seq...

In pmoulos/metaseqr: An R package for the analysis and result reporting of RNA-Seq data by combining multiple statistical algorithms.

Description

This function assembles gene models (single genes, not isoforms) based on the input read counts file (3' UTRs) and a gene annotation data frame, either from an external file provided by the user, or with the get.annotation function. The gene.data argument should have a specific format and for this reason it's better to use one of the two aforementioned ways to supply it. This function is intended mostly for internal use but can be used if the requirements are met.

Usage

    construct.utr.model(utr.counts, sample.list, gene.data,
        multic = FALSE)

Arguments

utr.counts	the exon counts data frame produced by reading the exon read counts file.
sample.list	the list containing condition names and the samples under each condition.
gene.data	an annotation data frame from the same organism as exon.counts (such the ones produced by get.annotation).
multic	a logical value indicating the presence of multiple cores. Defaults to FALSE. Do not change it if you are not sure whether package multicore has been loaded or not.

Value

A named list where names represent samples. Each list member is a also a named list where names correspond to gene ids and members are named vectors. Each vector is named according to the exons corresponding to each gene and contains the read counts for each exon. This structure is used for exon filtering and assembling final gene counts in the metaseqr pipeline.

Author(s)

Panagiotis Moulos

Examples

# Takes some time to run...
data("hg19.exon.data",package="metaseqR")
gene.data <- get.annotation("hg19","gene","ensembl")
reduced.gene.data <- reduce.gene.data(hg19.exon.counts,
    gene.data)
multic <- check.parallel(0.4)
gene.model <- construct.utr.model(hg19.exon.counts,
    sample.list.hg19,gene.data,multic)

pmoulos/metaseqr documentation built on Dec. 29, 2020, 5:56 a.m.