results_topTable: Calculate results

Description Usage Arguments Value Author(s) See Also Examples

View source: R/results_topTable.R

Description

Calculate results

Usage

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results_topTable(lm2.contrast, expr.toBind, pvalue = 0.05, logFC = 1,
  typeID = "ensembl_gene_id", genes_annotation_unique, annotations,
  adjust = "no")

Arguments

lm2.contrast

MArrayLM object

expr.toBind

Expression data.matrix with supplemental colums: module and ID

pvalue

p-value limit (alpha)

logFC

log2 fold change limit #VERIFY IT IS REALLY LOG2 (default = 1)

typeID

The type of ID used (default="ensembl_gene_id")

genes_annotation_unique

All the annotations for every ID in the 2nd row in expr.toBind (or rownames of expr.matrix)

annotations

Annotation (???)

adjust

Which correction for multiple analysis to use (default = "no"). Note: None is different than no somehow

Value

results

topTable of only the significant results

topTable3

Complete topTable

Author(s)

Simon J Pelletier

See Also

topTable , MArrayLM , transcript_count , expr.toBind

Examples

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expr.matrix <- readRDS("data/expr_matrix_LGVD.rds")
design <- design_contrasts(get_names(colnames(expr.matrix)))
results_list <- results_topTable()
lm2 <- lm2Contrast(expr.matrix,design)
lm2.contrast = lm2[[1]]
contrasts=lm2[[2]]
contrast.matrix=lm2[[3]]

spell098/rnaseq_app documentation built on May 30, 2019, 7:57 a.m.