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J Theor Biol ; 589: 111850, 2024 07 21.
Artigo em Inglês | MEDLINE | ID: mdl-38740126

RESUMO

Protein-protein interactions (PPIs) are crucial for various biological processes, and predicting PPIs is a major challenge. To solve this issue, the most common method is link prediction. Currently, the link prediction methods based on network Paths of Length Three (L3) have been proven to be highly effective. In this paper, we propose a novel link prediction algorithm, named SMS, which is based on L3 and protein similarities. We first design a mixed similarity that combines the topological structure and attribute features of nodes. Then, we compute the predicted value by summing the product of all similarities along the L3. Furthermore, we propose the Max Similarity Multiplied Similarity (maxSMS) algorithm from the perspective of maximum impact. Our computational prediction results show that on six datasets, including S. cerevisiae, H. sapiens, and others, the maxSMS algorithm improves the precision of the top 500, area under the precision-recall curve, and normalized discounted cumulative gain by an average of 26.99%, 53.67%, and 6.7%, respectively, compared to other optimal methods.


Assuntos
Algoritmos , Mapeamento de Interação de Proteínas , Mapas de Interação de Proteínas , Humanos , Mapeamento de Interação de Proteínas/métodos , Biologia Computacional/métodos , Saccharomyces cerevisiae/metabolismo , Saccharomyces cerevisiae/genética , Bases de Dados de Proteínas , Proteínas de Saccharomyces cerevisiae/metabolismo , Proteínas de Saccharomyces cerevisiae/genética
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