Skip to main content
Bioinformatics logoLink to Bioinformatics
. 2018 Jul 19;34(23):4139. doi: 10.1093/bioinformatics/bty515

Distinguishing prognostic and predictive biomarkers: an information theoretic approach

Konstantinos Sechidis, Konstantinos Papangelou, Paul D Metcalfe, David Svensson, James Weatherall, Gavin Brown
PMCID: PMC6247935  PMID: 30052765

Bioinformatics, (2018) https://doi.org/10.1093/bioinformatics/bty357

The author wishes to apologize for a mistake in Figure 2 in the above manuscript. The figure appears correctly below:

Fig. 2.

Fig. 2.

When biomarkers have both prognostic/predictive strength (M-1) VT achieves higher TPR, otherwise (M-2) the gains in TPR are vanishing. In terms of FNRProg., VT always has very high error rate on selecting solely prognostic biomarkers as predictive, and it performs worse than random selection. This is the average TPR/FNRProg. over 200 simulated datasets for three different values of the predictive strength θ: 1/5 means a strongly prognostic signal, 1 means equal strength between prognostic and predictive signals, and 5 means a strongly predictive signal. The sample size is 2000, and the dimensionality p = 30 biomarkers. Dashed lines show the TPR/FNRProg. if we were ranking the biomarkers at random. (a) M-1: Biomarkers can be both prognostic and predictive. (b) M-2: Biomarkers are solely either prognostic or predictive

The paper has been corrected online.


Articles from Bioinformatics are provided here courtesy of Oxford University Press

RESOURCES