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Myocardial perfusion imaging (MPI) using single photon emission computed tomography (SPECT) has been shown to have good prognostic power for diagnosing coronary artery disease [1, 2].
Numerous of these 'signatures' show good prognostic power, but surprisingly gene-wise overlap between them has been minimal (Ein-Dor et al, 2006; Fan et al, 2006; Chen et al, 2007; Lau et al, 2007), which increases the difficulty of introducing microarrays in clinical practice.
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Validation of the mathematical models with 4 runs indicated the good prognostic ability of Resolution IV design.
This gene signature shows a good prognostic ability to discriminate colorectal cancer patients between good and poor prognostic groups with high accuracy [ 14].
Ki-67 had good prognostic discriminating power irrespective of the cut-point value, but S-phase fraction lost its prognostic power at higher cut-point values.
We were not the first to find that a 1-gene signature had an equally good or stronger prognostic power than a gene signatures with a higher number of genes.
Both scales provided good predictive power and exhibited good efficiency.
This equation had good predictive power (R = 0.76).
arabiensis attesting the good predictive power of the model.
Both scales were found to have good predictive power and exhibited good efficiency.
Patients within the good prognostic group (Nottingham Prognostic Index (NPI) ≤ 3.4) did not receive adjuvant therapy (AT).
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