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Table 2 Summary of quality measures for temperature calibration.

From: The impact of quantitative optimization of hybridization conditions on gene expression analysis

Hyb. Temp., k

accfly

I fly

n sig

accspk

I spk

Hyb 47 C

71.74

0.405

-67616

2925

71.05

0.106

-19780

Hyb 49 C

72.25

0.417

-65697

1979

74.14

0.234

-16810

Hyb 50 C (a)

74.06

0.451

-60972

3201

71.94

0.133

-18930

Hyb 50 C (b)

75.05

0.461

-60111

3628

73.28

0.261

-16454

Hyb 51 C

75.06

0.467

-58616

3810

74.10

0.341

-14683

Hyb 52 C

71.79

0.402

-68745

2140

73.16

0.156

-18357

Hyb 54 C

70.35

0.385

-70643

2348

68.34

0.184

-18371

Hyb 56 C

64.25

0.292

-83426

1213

60.64

0.094

-20323

  1. The left part of the table shows results from the protocol assessment using biological samples for calibration ('fly'). In comparison, the corresponding results for spiked-in exogenic RNAs are shown on the right ('spk'). Column 'Hyb. Temp., K' lists the considered protocol K and its hybridization temperature. For each protocol, the table displays the achieved generalization accuracies ('acc'), the average mutual information I, the log likelihoods log and the number n of genes with differential expression calls by FSPMA ANOVA at a 1% FDR threshold. The generalization accuracy reflects protocol performance for equal misclassification costs. ROC curves are provided for the generic case (Fig. 4). Detailed results for each protocol can be found in the Supplement.