Package 'mimager'

Title: mimager: The Microarray Imager
Description: Easily visualize and inspect microarrays for spatial artifacts.
Authors: Aaron Wolen [aut, cre, cph]
Maintainer: Aaron Wolen <[email protected]>
License: MIT + file LICENSE
Version: 1.31.0
Built: 2024-12-04 06:01:33 UTC
Source: https://github.com/bioc/mimager

Help Index


Array rank

Description

Determines the rank of values within each matrix of a three-dimensional array.

Usage

arank(x, na.last = TRUE, ties.method = "first")

Arguments

x

a three-dimensional array of matrices

na.last

for controlling the treatment of NAs. If TRUE, missing values in the data are put last; if FALSE, they are put first; if NA, they are removed; if "keep" they are kept with rank NA.

ties.method

a character string specifying how ties are treated, see ‘Details’; can be abbreviated.

Value

an array with the same dimensions as x

See Also

rank

Other array.transformations: arle

Examples

# microarray visualization
if (require(affydata, quietly = TRUE)) {
  data("Dilution", package = "affydata")
  x <- arank(marray(Dilution, transpose = TRUE))
}

Array relative log expression

Description

The relative log expression (RLE) quantifies the extent to which each sample in a dataset differs from a "reference" sample, which represents each probe's median value across all samples.

Usage

arle(x, log2 = TRUE, normalize = TRUE)

Arguments

x

a three-dimensional array of matrices

log2

should values be $log_2$ transformed

normalize

should values be quantile normalized

Value

an array with the same dimensions as x

See Also

RLE

Other array.transformations: arank

Examples

# microarray visualization
if (require(affydata, quietly = TRUE)) {
  data("Dilution", package = "affydata")
  x <- arle(marray(Dilution, transpose = TRUE))
}

Microarray array

Description

Convert S4 microarray data structures into a three-dimensional array of matrices, where each matrix corresponds to an individual sample's microarray with values arranged to reflect the physical position of the corresponding feature (i.e., probe) on the microarray surface.

Usage

marray(object, type = NULL, select = NULL, transpose = NULL)

## S4 method for signature 'AffyBatch'
marray(object, type = "pm", select = NULL,
  transpose = FALSE)

## S4 method for signature 'PLMset'
marray(object, type = "residuals", select = NULL,
  transpose = FALSE)

## S4 method for signature 'FeatureSet'
marray(object, type = "pm", select = NULL,
  transpose = FALSE)

## S4 method for signature 'oligoPLM'
marray(object, type = "residuals", select = NULL,
  transpose = FALSE)

Arguments

object

a valid Bioconductor microarray data structure

type

for microarray objects type refers to probe type; for objects containing probe-level models (e.g., PLMsets) type refers to the value type (i.e, "residuals" or "weights"). See probe type section for more information.

select

a numeric, character or logical vector indicating samples to include

transpose

TRUE (the default), ensures the reconstructed microarrays are vertically oriented, as is typically expected. Set to FALSE to return an array in the orientation strictly specified by the platform coordinates

Value

three-dimensional array

Probe types

For microarray data structures the type argument determines the type of probe that should be included. The following table provides a list of valid values for each supported microarray class:

AffyBatch "all" "pm" "mm" -
ExpressionFeatureSet "all" "pm" "mm" -
GeneFeatureSet "all" "pm" - "bg"
ExonFeatureSet "all" "pm" "mm" "bg"
SnpFeatureSet "all" "pm" "mm" -

Examples

if (require(affydata, quietly = TRUE)) {
  data("Dilution", package = "affydata")
  dilution.array <- marray(Dilution, select = c("20A", "10A"))
}

Microarray image

Description

Visualize microarray probe intensities arranged by their physical location on the array. A false color image is produced for each sample in the microarray object and arranged in a grid.

Usage

mimage(object, type = NULL, select = NULL, colors = NULL,
  legend.label = NULL, nrow = NULL, ncol = NULL, fixed = FALSE,
  empty.rows = "fill", empty.thresh = 0.6, transform = NULL,
  trim = 0.01, fontsize = 12)

## S4 method for signature 'AffyBatch'
mimage(object, type = "pm", select = NULL,
  colors = NULL, legend.label = "Intensity", nrow = NULL, ncol = NULL,
  fixed = FALSE, empty.rows = "fill", empty.thresh = 0.6,
  transform = log2, trim = 0.01, fontsize = 12)

## S4 method for signature 'PLMset'
mimage(object, type = "residuals", select = NULL,
  colors = NULL, legend.label = type, nrow = NULL, ncol = NULL,
  fixed = FALSE, empty.rows = "fill", empty.thresh = 0.6,
  transform = identity, trim = 0.01, fontsize = 12)

## S4 method for signature 'FeatureSet'
mimage(object, type = "pm", select = NULL,
  colors = NULL, legend.label = "Intensity", nrow = NULL, ncol = NULL,
  fixed = FALSE, empty.rows = "fill", empty.thresh = 0.6,
  transform = log2, trim = 0.01, fontsize = 12)

## S4 method for signature 'oligoPLM'
mimage(object, type = "residuals", select = NULL,
  colors = NULL, legend.label = type, nrow = NULL, ncol = NULL,
  fixed = FALSE, empty.rows = "fill", empty.thresh = 0.6,
  transform = identity, trim = 0.01, fontsize = 12)

## S4 method for signature 'array'
mimage(object, type = NULL, select = NULL,
  colors = NULL, legend.label = "Values", nrow = NULL, ncol = NULL,
  fixed = FALSE, empty.rows = "ignore", empty.thresh = 1,
  transform = identity, trim = 0, fontsize = 12)

Arguments

object

a valid Bioconductor microarray data structure

type

for microarray objects type refers to probe type; for objects containing probe-level models (e.g., PLMsets) type refers to the value type (i.e, "residuals" or "weights"). See probe type section for more information.

select

a numeric, character or logical vector indicating samples to include

colors

a vector of colors used to represent probe values

legend.label

Legend label

nrow

optional, number of rows in grid layout

ncol

optional, number of columns in grid layout

fixed

Force images to assume a fixed aspect ratio corresponding to their physical dimensions

empty.rows

Should empty rows be filled with values from neighboring rows (the default, "fill"), should they be dropped ("drop") entirely, or should they be left alone ("ignore")

empty.thresh

what proportion of features must be missing from a row to consider that row empty

transform

a function to be applied to the values prior to visualizatio

trim

a percentile (default = 0.02) or range or 2 values see trimming section for details

fontsize

font size for labels and legend

Value

invisibly a gtable matrix of grobs

Trimming

By default, a 98% winsorization is performed prior to visualization, pulling in values outside of the 1st and 99th percentiles to their respective endpoints. This can be modified using the trim argument to provide either a new percentile, or a range of 2 values defining the min/max of the trimmed endpoints. Set trim = 0 to avoid trimming entirely.

Empty Rows

As a result of platform design, the presence unindexed probes or probe selection by the user (e.g., including only "pm" probes), the matrix-representation of a microarray can contain numerous rows comprised entirely (or mostly) of missing values, which may produce undesirable rasterization artifacts in the microarray image. To avoid this, empty rows are filled with values from a neighboring row. The threshold for what constitutes an empty row can be tweaked with the empty.thresh argument.

Probe types

For microarray data structures the type argument determines the type of probe that should be included. The following table provides a list of valid values for each supported microarray class:

AffyBatch "all" "pm" "mm" -
ExpressionFeatureSet "all" "pm" "mm" -
GeneFeatureSet "all" "pm" - "bg"
ExonFeatureSet "all" "pm" "mm" "bg"
SnpFeatureSet "all" "pm" "mm" -

Examples

# standard array visualization
mimage(iris3)

# microarray visualization
if (require(affydata, quietly = TRUE)) {
  data("Dilution", package = "affydata")
  mimage(Dilution, select = c("20A", "10A"))
}

mimager: The Microarray Imager

Description

mimager simplifies the creation of microarray images (sometimes called "pseudo-images") for the purpose of identifying problematic regional aberrations. Notable features include support for many of Bioconductor's core microarray data structures, providng compatibility with a variety of common microarray platforms, and the ability to visualize multiple microarrays simultaneously.

Details

The following Bioconductor microarray data structures are currently supported:

  • AffyBatch-class for Affymetrix GeneChip probe level data

  • PLMset-class for probe-level linear models fitted to Affymetrix GeneChip probe level data

  • FeatureSet-class for storing Expression/Exon/SNP data from a variety of oligonucleotide platforms

  • oligoPLM-class for probe-level linear models fitted to any of the FeatureSet-like classes