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Table 1 An overview of the results for the two spike-in experiments

From: Delineation of amplification, hybridization and location effects in microarray data yields better-quality normalization

(ROC50 scores)

HG_U95A

HG_U133A

Method name

fold chg. single repl.

SAM all

fold chg. all

fold chg. single repl.

SAM all

fold chg. all

MAS 5.0

0.00

0.25

0.01

0.01

0.45

0.02

PLIER

0.00

0.49

0.01

0.04

0.61

0.10

VSN

0.62

0.42

0.77

0.65

0.32

0.70

PDNN

0.63

0.45

0.73

0.59

0.70

0.71

RMA_NBG

0.64

0.53

0.78

0.69

0.66

0.77

RMA

0.47

0.27

0.75

0.68

0.70

0.77

GCRMA

0.71

0.68

0.84

0.65

0.57

0.72

RDN

0.80

0.66 (0.76)

0.89

0.75

0.77

0.80

RDN [qq]

0.67

0.57

0.80

0.71

0.65

0.77

RDN [qq, loc]

0.70

0.65

0.83

0.72

0.69

0.78

RDN [qq, hyb]

0.76

0.74

0.87

0.75

0.75

0.80

RDN [qq, hyb, amp]

0.76

0.73

0.87

0.75

0.75

0.80

RDN [qq, hyb, loc]

0.80

0.68

0.88

0.76

0.77

0.80

  1. See Additional file 1, Table S1 for a description of the methods. Both fold change and the SAM test statistic were used to determine ROC50 scores (see Methods section). The 'single repl.' score is determined by applying the normalization and scoring methods to each of the three replicate array-sets individually and averaging the results, while the 'all' score is obtained by using all replicates simultaneously. The lower 5 rows describe versions of RDN which use a subset of quantile-quantile normalization ('qq'), array location ('loc'), hybridization ('hyb') and amplification ('amp') correction to determine their individual influence.