Evidence map›Paper›PMID 34807960›Full record

ArticlePloS one2021

Fusion of KATZ measure and space projection to fast probe potential lncRNA-disease associations in bipartite graphs.

Yi Zhang, Min Chen, Li Huang, Xiaolan Xie, Xin Li, Hong Jin, Xiaohua Wang, Hanyan Wei

Abstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yi ZhangSchool of Information Science and Engineering, Guilin University of Technology, Guilin, China.ORCID 0000-0001-6167-7945
Min ChenSchool of Computer Science and Technology, Hunan Institute of Technology, Hengyang, China.ORCID 0000-0002-7019-9102
Li HuangAcademy of Arts and Design, Tsinghua University, Beijing, China.
Xiaolan XieSchool of Information Science and Engineering, Guilin University of Technology, Guilin, China.
Xin LiSchool of Information Science and Engineering, Guilin University of Technology, Guilin, China.
Hong JinSchool of Information Science and Engineering, Guilin University of Technology, Guilin, China.
Xiaohua WangPharmacy School, Guilin Medical University, Guilin, China.
Hanyan WeiPharmacy School, Guilin Medical University, Guilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well known that numerous long noncoding RNAs (lncRNAs) closely relate to the physiological and pathological processes of human diseases and can serves as potential biomarkers. Therefore, lncRNA-disease associations that are identified by computational methods as the targeted candidates reduce the cost of biological experiments focusing on deep study furtherly. However, inaccurate construction of similarity networks and inadequate numbers of observed known lncRNA-disease associations, such inherent problems make many mature computational methods that have been developed for many years still exit some limitations. It motivates us to explore a new computational method that was fused with KATZ measure and space projection to fast probing potential lncRNA-disease associations (namely KATZSP). KATZSP is comprised of following key steps: combining all the global information with which to change Boolean network of known lncRNA-disease associations into the weighted networks; changing the similarities calculation into counting the number of walks that connect lncRNA nodes and disease nodes in bipartite graphs; obtaining the space projection scores to refine the primary prediction scores. The process to fuse KATZ measure and space projection was simplified and uncomplicated with needing only one attenuation factor. The leave-one-out cross validation (LOOCV) experimental results showed that, compared with other state-of-the-art methods (NCPLDA, LDAI-ISPS and IIRWR), KATZSP had a higher predictive accuracy shown with area-under-the-curve (AUC) value on the three datasets built, while KATZSP well worked on inferring potential associations related to new lncRNAs (or isolated diseases). The results from real cases study (such as pancreas cancer, lung cancer and colorectal cancer) further confirmed that KATZSP is capable of superior predictive ability to be applied as a guide for traditional biological experiments.

Indexed as

AlgorithmsGene Regulatory NetworksGenetic Predisposition to DiseaseHumansModels, GeneticNeoplasmsRNA, Long NoncodingRNA, Long Noncoding

Identifiers

PMID34807960
PMCPMC8608294

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.