importLrrBaf {CNVRanger} | R Documentation

## Import LRR and BAF from text files used in the CNV analysis

### Description

This function imports the LRR/BAF values and create a node for each one in the GDS file at the working folder 'Inputs' created by the `setupCnvGWAS` function. Once imported, the LRR values can be used to perform a GWAS directly as an alternative to copy number dosage

### Usage

    importLrrBaf(
      all.paths,
      path.files,
      list.of.files,
      gds.file = NULL,
      verbose = TRUE
    )

### Arguments

`all.paths` | Object returned from `CreateFolderTree` function with the working folder tree
`path.files` | Folder containing the input CNV files used for the CNV calling (i.e. one text file with 5 collumns for each sample). Columns should contain (i) probe name, (ii) Chromosome, (iii) Position, (iv) LRR, and (v) BAF.
`list.of.files` | Data-frame with two columns where the (i) is the file name with signals and (ii) is the correspondent name of the sample in the gds file
`gds.file` | Path to the GDS file which contains nodes harboring respective LRR and BAF values. The ‘snp.rs.id’, ‘sample.id’, ‘LRR’ and ‘BAF’ nodes are mandatory. Both the SNPs and samples should follow the order and length in the CNV.gds (located at all.paths["Inputs"] folder). ‘path.files’ and ‘list.of.files’ will be ignored if ‘gds.file’ is not NULL
`verbose` | Print the samples while importing

### Value

Writes to the specified GDS file by side effect.

### Author(s)

Vinicius Henrique da Silva <vinicius.dasilva@wur.nl>

### Examples

    # Load phenotype-CNV information
    data.dir <- system.file("extdata", package="CNVRanger")

    phen.loc <- file.path(data.dir, "Pheno.txt")
    cnv.out.loc <- file.path(data.dir, "CNVOut.txt")
    map.loc <- file.path(data.dir, "MapPenn.txt")

    phen.info <- setupCnvGWAS('Example', phen.loc, cnv.out.loc, map.loc)

    # Extract path names
    all.paths <- phen.info$all.paths

    # List files to import LRR/BAF
    list.of.files <- list.files(path=data.dir, pattern="cnv.txt.adjusted$")
    list.of.files <- as.data.frame(list.of.files)
    colnames(list.of.files)[1] <- "file.names"
    list.of.files$sample.names <- sub(".cnv.txt.adjusted$", "", list.of.files$file.names)

    # All missing samples will have LRR = '0' and BAF = '0.5' in all SNPs listed in the GDS file
    importLrrBaf(all.paths, data.dir, list.of.files)

    # Read the GDS to check if the LRR/BAF nodes were added
    cnv.gds <- file.path(all.paths["Inputs"], 'CNV.gds')
    genofile <- SNPRelate::snpgdsOpen(cnv.gds, allow.fork=TRUE, readonly=FALSE)
    SNPRelate::snpgdsClose(genofile)

[Package CNVRanger version 1.8.0 Index]