Organism: Homo sapiens
Reference(s): 21254160 (Filter by genes in paper)    
Microarray quality metrics report for E-GEOD-23031 on array design A-AFFY-44

Microarray quality metrics report for E-GEOD-23031 on array design A-AFFY-44

- Array metadata and outlier detection overview
1GSM568466GSM568466ribavirin, 100 microgram per milliliterGSM568466.CEL
2GSM568468GSM568468ribavirin, 100 microgram per milliliterGSM568468.CEL
3GSM568467GSM568467ribavirin, 100 microgram per milliliterGSM568467.CEL
4GSM568464GSM568464phosphate buffered salineGSM568464.CEL
5GSM568463GSM568463phosphate buffered salineGSM568463.CEL
6GSM568465xGSM568465phosphate buffered salineGSM568465.CEL

The columns named *1, *2, ... indicate the calls from the different outlier detection methods:
  1. outlier detection by Boxplots
  2. outlier detection by Distances between arrays
  3. outlier detection by MA plots
The outlier detection criteria are explained below in the respective sections. Arrays that were called outliers by at least one criterion are marked by checkbox selection in this table, and are indicated by highlighted lines or points in some of the plots below. By clicking the checkboxes in the table, or on the corresponding points/lines in the plots, you can modify the selection. To reset the selection, reload the HTML page in your browser.

At the scope covered by this software, outlier detection is a poorly defined question, and there is no 'right' or 'wrong' answer. These are hints which are intended to be followed up manually. If you want to automate outlier detection, you need to limit the scope to a particular platform and experimental design, and then choose and calibrate the metrics used.

Section 1: Array intensity distributions

- Figure 1: Boxplots.
Figure 1 (PDF file) shows boxplots representing summaries of the signal intensity distributions of the arrays. Each box corresponds to one array. Typically, one expects the boxes to have similar positions and widths. If the distribution of an array is very different from the others, this may indicate an experimental problem. Outlier detection was performed by computing the Kolmogorov-Smirnov statistic Ka between each array's distribution and the distribution of the pooled data.

+ Figure 2: Outlier detection for Boxplots.
- Figure 3: Density plots.
phosphate buffered saline ribavirin, 100 microgram per milliliter Density 0.0 0.2 0.4 0.6 6 8 10 12

Figure 3 (PDF file) shows density estimates (smoothed histograms) of the data. Typically, the distributions of the arrays should have similar shapes and ranges. Arrays whose distributions are very different from the others should be considered for possible problems. Various features of the distributions can be indicative of quality related phenomena. For instance, high levels of background will shift an array's distribution to the right. Lack of signal diminishes its right right tail. A bulge at the upper end of the intensity range often indicates signal saturation.

Section 2: Between array comparison

- Figure 4: Distances between arrays.
Figure 4 (PDF file) shows a false color heatmap of the distances between arrays. The color scale is chosen to cover the range of distances encountered in the dataset. Patterns in this plot can indicate clustering of the arrays either because of intended biological or unintended experimental factors (batch effects). The distance dab between two arrays a and b is computed as the mean absolute difference (L1-distance) between the data of the arrays (using the data from all probes without filtering). In formula, dab = mean | Mai - Mbi |, where Mai is the value of the i-th probe on the a-th array. Outlier detection was performed by looking for arrays for which the sum of the distances to all other arrays, Sa = Σb dab was exceptionally large. No such arrays were detected.

+ Figure 5: Outlier detection for Distances between arrays.
- Figure 6: Principal Component Analysis.
phosphate buffered saline ribavirin, 100 microgram per milliliter PC1 PC2 -300 -200 -100 0 100 -300 -200 -100 0 100 200 300

Figure 6 (PDF file) shows a scatterplot of the arrays along the first two principal components. You can use this plot to explore if the arrays cluster, and whether this is according to an intended experimental factor, or according to unintended causes such as batch effects. Move the mouse over the points to see the sample names.
Principal component analysis is a dimension reduction and visualisation technique that is here used to project the multivariate data vector of each array into a two-dimensional plot, such that the spatial arrangement of the points in the plot reflects the overall data (dis)similarity between the arrays.

Section 3: Individual array quality

- Figure 7: MA plots.
Figure 7 (PDF file) shows MA plots. M and A are defined as:
M = log2(I1) - log2(I2)
A = 1/2 (log2(I1)+log2(I2)),
where I1 is the intensity of the array studied,and I2 is the intensity of a "pseudo"-array that consists of the median across arrays. Typically, we expect the mass of the distribution in an MA plot to be concentrated along the M = 0 axis, and there should be no trend in M as a function of A. If there is a trend in the lower range of A, this often indicates that the arrays have different background intensities; this may be addressed by background correction. A trend in the upper range of A can indicate saturation of the measurements; in mild cases, this may be addressed by non-linear normalisation (e.g. quantile normalisation).
Outlier detection was performed by computing Hoeffding's statistic Da on the joint distribution of A and M for each array. The value of Da is shown in the panel headings. 0 arrays had Da>0.15 and were marked as outliers. For more information on Hoeffing's D-statistic, please see the manual page of the function hoeffd in the Hmisc package.

+ Figure 8: Outlier detection for MA plots.

This report has been created with arrayQualityMetrics 3.26.1 under R version 3.2.3 (2015-12-10).

(Page generated on Tue May 17 13:53:45 2016 by hwriter )