Description Usage Arguments Value Examples
View source: R/function_PCA.Analysis.R
Generate plot for Principal Component Analysis
1 2 3 4 5 6 7 8 9 10 11 12  | pca_analysis(
  tool,
  name,
  work_dir,
  pair_name = "G2_over_G1",
  width = 4,
  height = 2,
  res = 300,
  unit = "in",
  image_format = "png",
  env
)
 | 
tool | 
 A character string indicating which differential expression analysis tool was last used.  | 
name | 
 A character string indicating the desired values to be used in next analysis. For instance, "HIF3A" in the legacy gene expression matrix, "mir-1307" in the miRNA quantification matrix, or "HER2" in the protein quantification matrix.  | 
work_dir | 
 A character string specifying the path to work directory.  | 
pair_name | 
 A character string indicating which condition name should be
used. When there are only two groups the default is   | 
width | 
 Graphical parameters. See par for more
details. As default   | 
height | 
 Graphical parameters. See par for more
details. As default   | 
res | 
 Graphical parameters. See par for more
details. As default   | 
unit | 
 Graphical parameters. See par for more
details. As default   | 
image_format | 
 A character string indicating which image_format will be used. It could be "png" or "svg". The only unit available in "svg" is inches ('in'). The default is "png".  | 
env | 
 A character string containing the environment name that should be used. If none has been set yet, the function will create one in global environment following the standard criteria: 
  | 
the PCAs plots.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40  | library(DOAGDC)
# data already downloaded using the 'download_gdc' function
concatenate_expression("gene",
   name = "HIF3A",
   data_base = "legacy",
   tumor = "CHOL",
   work_dir = "~/Desktop"
)
# separating gene HIF3A expression data patients in two groups
groups_identification_mclust("gene", 2,
   name = "HIF3A",
   modelName = "E",
   env = CHOL_LEGACY_gene_tumor_data,
   tumor = "CHOL"
)
# load not normalized data
concatenate_expression("gene",
   normalization = FALSE,
   name = "HIF3A",
   data_base = "legacy",
   tumor = "CHOL",
   env = CHOL_LEGACY_gene_tumor_data,
   work_dir = "~/Desktop"
)
# start DE analysis
# considering concatenate_expression and groups_identification already runned
dea_edger(
   name = "HIF3A",
   group_gen = "mclust",
   env = CHOL_LEGACY_gene_tumor_data
)
pca_analysis("edgeR", "HIF3A", "~/Desktop",
   pair_name = "G2_over_G1",
   env = CHOL_LEGACY_gene_tumor_data
)
 | 
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