ABSTRACT:
Next generation Affymetrix tiling microarrays
often have
blob-like image defects that will require investigators to either
repeat their hybridization
assays or analyze their data with the defects still present. We
investigated
the effect of analyzing ENCODE spike-in genome tiling array data in the
presence of simulated blobs covering between 1 and 9% of the array
area. Using
two different tiling array analysis programs (Affymetrix
Tiling Array Software TAS
and Model-based
Analysis for Tiling arrays MAT), we found that even the
smallest
blob defects significantly decreased the sensitivity and increased
false
discovery rate (FDR) in a tiling array
spike-in analysis.
We introduce a new software tool, the Microarray Blob
Remover (MBR), which allows rapid visualization, detection, and
removal of blob
defects of a variety of sizes and shapes from different types of
microarrays
using their .CEL files. Removal of the affected probes in the
blob-defects using
MBR was shown to significantly improve sensitivity and FDR compared to
leaving
the affected probes in the analysis.
DATA:
EXAMPLE
DEFECT Affymetrix .CEL files:
A) Expression
Array
B) SNP Array
C) Genome
Tiling Array2
D) Promoter
Array
ENCODE ARRAY
FILES (released Aug 8, 2006):
Full series of arrays (GEO
Accession number GSE5053)
Spike-in array (GEO
Accession number GSM113413)
and
corresponding Genomic Control Input array (GEO Accession number GSM113420)
SAMPLE SIMULATED
FILES:
Single Blob-Defect of size p% placed in 1 of 3x3 squares
1% Defect
in Location 1,1
5% Defect
in Location 1,3
9% Defect
in Location 3,2