An Iterative Distance-Based Model for Unsupervised Weighted Rank Aggregation

Author(s):  
Leonidas Akritidis ◽  
Athanasios Fevgas ◽  
Panayiotis Bozanis
2018 ◽  
Vol 149 ◽  
pp. 47-60 ◽  
Author(s):  
Sujoy Chatterjee ◽  
Anirban Mukhopadhyay ◽  
Malay Bhattacharyya

2009 ◽  
Vol 10 (1) ◽  
pp. 62 ◽  
Author(s):  
Vasyl Pihur ◽  
Susmita Datta ◽  
Somnath Datta

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Jianlong Qi ◽  
Tom Michoel ◽  
Gregory Butler

The module network method, a special type of Bayesian network algorithms, has been proposed to infer transcription regulatory networks from gene expression data. In this method, a module represents a set of genes, which have similar expression profiles and are regulated by same transcription factors. The process of learning module networks consists of two steps: first clustering genes into modules and then inferring the regulation program (transcription factors) of each module. Many algorithms have been designed to infer the regulation program of a given gene module, and these algorithms show very different biases in detecting regulatory relationships. In this work, we explore the possibility of integrating results from different algorithms. The integration methods we select are union, intersection, and weighted rank aggregation. Experiments in a yeast dataset show that the union and weighted rank aggregation methods produce more accurate predictions than those given by individual algorithms, whereas the intersection method does not yield any improvement in the accuracy of predictions. In addition, somewhat surprisingly, the union method, which has a lower computational cost than rank aggregation, achieves comparable results as given by rank aggregation.


Cancers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 917
Author(s):  
Jun A ◽  
Baotong Zhang ◽  
Zhiqian Zhang ◽  
Hailiang Hu ◽  
Jin-Tang Dong

Molecular signatures predictive of recurrence-free survival (RFS) and castration resistance are critical for treatment decision-making in prostate cancer (PCa), but the robustness of current signatures is limited. Here, we applied the Robust Rank Aggregation (RRA) method to PCa transcriptome profiles and identified 287 genes differentially expressed between localized castration-resistant PCa (CRPC) and hormone-sensitive PCa (HSPC). Least absolute shrinkage and selection operator (LASSO) and stepwise Cox regression analyses of the 287 genes developed a 6-gene signature predictive of RFS in PCa. This signature included NPEPL1, VWF, LMO7, ALDH2, NUAK1, and TPT1, and was named CRPC-derived prognosis signature (CRPCPS). Interestingly, three of these 6 genes constituted another signature capable of distinguishing CRPC from HSPC. The CRPCPS predicted RFS in 5/9 cohorts in the multivariate analysis and remained valid in patients stratified by tumor stage, Gleason score, and lymph node status. The signature also predicted overall survival and metastasis-free survival. The signature’s robustness was demonstrated by the C-index (0.55–0.74) and the calibration plot in all nine cohorts and the 3-, 5-, and 8-year area under the receiver operating characteristic curve (0.67–0.77) in three cohorts. The nomogram analyses demonstrated CRPCPS’ clinical applicability. The CRPCPS thus appears useful for RFS prediction in PCa.


2020 ◽  
Vol 11 (2) ◽  
pp. 1-33
Author(s):  
Haibing Lu ◽  
Xi Chen ◽  
Junmin Shi ◽  
Jaideep Vaidya ◽  
Vijayalakshmi Atluri ◽  
...  

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