On the Normal-Selection Model

1997 ◽  
pp. 309-320
Author(s):  
S. N. Ethier
Keyword(s):  
Selection Model

OPTIMIZATION OF ATTRIBUTE SELECTION MODEL USING BIO-INSPIRED ALGORITHMS

2019 ◽  
Vol 18 (1) ◽  
pp. 35-55
Author(s):  
Mohammad Aizat Basir ◽  
Yuhanis Yusof ◽  
Mohamed Saifullah Hussin
Keyword(s):  
Selection Model ◽  
Attribute Selection

Adaptive Component Replica Selection Model and Algorithms

2008 ◽  
Vol 19 (5) ◽  
pp. 1212-1223 ◽  
Author(s):  
Lin ZUO
Keyword(s):  
Selection Model ◽  
Replica Selection

A Service Selection Model Using Mixed Intelligent Optimization

2010 ◽  
Vol 33 (11) ◽  
pp. 2116-2125 ◽  
Author(s):  
Yan-Ping CHEN ◽  
Jian-Ke ZHANG ◽  
Jia-Ze SUN ◽  
Qing-Hua ZHENG ◽  
Zheng-Zhi LI
Keyword(s):  
Service Selection ◽  
Selection Model ◽  
Intelligent Optimization

A Sequential Recommendation - Selection Model

2019 ◽  
Author(s):  
Ningyuan Chen ◽  
Guillermo Gallego ◽  
Pin Gao ◽  
Anran Li
Keyword(s):  
Selection Model

Pathogenic Genes Selection Model of Genetic Disease based on Network Motifs Slicing Feedback

2019 ◽  
Vol 16 (5) ◽  
pp. 392-401
Author(s):  
Shengli Zhang ◽  
Zekun Tong ◽  
Haoyu Yin ◽  
Yifan Feng
Keyword(s):  
Genetic Disease ◽  
Drug Targets ◽  
Selection Model ◽  
Network Motifs ◽  
Gene Set ◽  
Pathway Network ◽  
Gene Pathway ◽  
Pathogenic Genes ◽  
Pathogenic Gene ◽  
Selection Of

Background: Finding the pathogenic gene is very important for understanding the pathogenesis of the disease, locating effective drug targets and improving the clinical level of medical treatment. However, the existing methods for finding the pathogenic genes still have limitations, for instance the computational complexity is high, and the combination of multiple genes and pathways has not been considered to search for highly related pathogenic genes and so on. Methods: We propose a pathogenic genes selection model of genetic disease based on Network Motifs Slicing Feedback (NMSF). We find a point set which makes the conductivity of the motif minimum then use it to substitute for the original gene pathway network. Based on the NMSF, we propose a new pathogenic genes selection model to expand pathogenic gene set. Results: According to the gene set we have obtained, selection of key genes will be more accurate and convincing. Finally, we use our model to screen the pathogenic genes and key pathways of liver cancer and lung cancer, and compare the results with the existing methods. Conclusion: The main contribution is to provide a method called NMSF which simplifies the gene pathway network to make the selection of pathogenic gene simple and feasible. The fact shows our result has a wide coverage and high accuracy and our model has good expeditiousness and robustness.

Sign in / Sign up

Export Citation Format

Share Document