modpar.new: Settings for multiSOMe analysis

Description Usage Arguments Value

View source: R/modpar_new.r

Description

Settings for multiSOMe analysis

Usage

1
modpar.new(modpar = NULL)

Arguments

dataset.name

all output will be stored in a folder with the name given

meth.type

type of Methylation Assay used. Either '27K' for Infinium HumanMethylation27K or 'K450' for Infinium HumanMethylation450K. If methylation data is already preprocessed and the data matrix contains methylation values per gene per sample set meth.type=""

w

weight used to either focus on gene expression (w=0), DNA methylation (w=1) or on both (w=0.5)

mean.norm.exp

enables centralization of the expression features (boolean)

mean.norm.meth

enables centralization of the methylation features (boolean)

quant.exp

enables quantile normalization of the expression samples (boolean)

quant.meth

enables quantile normalization of the expression samples (boolean)

M

enables calculation of M values out of methylation beta values (boolean)

row.ids.exp

type of rowname identifier in biomaRt database of gene expression matrix, for example 'ensembl_gene_id', "refseq_mrna" or 'external_gene_name'. For details see https://www.bioconductor.org/packages//2.7/bioc/vignettes/biomaRt/inst/doc/biomaRt.pdf

row.ids.meth

type of rowname identifier in biomaRt database of DNA methylation matrix, for example 'ensembl_gene_id', "refseq_mrna" or 'external_gene_name'. For details see https://www.bioconductor.org/packages//2.7/bioc/vignettes/biomaRt/inst/doc/biomaRt.pdf

return.ids

type of rowname identifier in biomaRt database to return, for example 'ensembl_gene_id' or 'external_gene_name'. For details see https://www.bioconductor.org/packages//2.7/bioc/vignettes/biomaRt/inst/doc/biomaRt.pdf

Value

modpar


lydiahopp/multiSOMe documentation built on Oct. 13, 2019, 2:06 p.m.