scholarly journals Multimorbidity prediction using link prediction

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Furqan Aziz ◽  
Victor Roth Cardoso ◽  
Laura Bravo-Merodio ◽  
Dominic Russ ◽  
Samantha C. Pendleton ◽  
...  

AbstractMultimorbidity, frequently associated with aging, can be operationally defined as the presence of two or more chronic conditions. Predicting the likelihood of a patient with multimorbidity to develop a further particular disease in the future is one of the key challenges in multimorbidity research. In this paper we are using a network-based approach to analyze multimorbidity data and develop methods for predicting diseases that a patient is likely to develop. The multimorbidity data is represented using a temporal bipartite network whose nodes represent patients and diseases and a link between these nodes indicates that the patient has been diagnosed with the disease. Disease prediction then is reduced to a problem of predicting those missing links in the network that are likely to appear in the future. We develop a novel link prediction method for static bipartite network and validate the performance of the method on benchmark datasets. By using a probabilistic framework, we then report on the development of a method for predicting future links in the network, where links are labelled with a time-stamp. We apply the proposed method to three different multimorbidity datasets and report its performance measured by different performance metrics including AUC, Precision, Recall, and F-Score.

Sensors ◽  
2020 ◽  
Vol 20 (22) ◽  
pp. 6560
Author(s):  
Hui Wang ◽  
Zichun Le

Link prediction is the most basic and essential problem in complex networks. This study analyzes the observed topological, time, attributive, label, weight, directional, and symbolic features and auxiliary information to find the lack of connection and predict the future possible connection. For discussion and analysis of the evolution of the network, the network model is of great significance. In the past two decades, link prediction has attracted extensive attention from experts in various fields, who have published numerous high-level papers, but few combine interdisciplinary characteristics. This survey analyzes and discusses the existing link prediction methods. The idea of stratification is introduced into the classification system of link prediction for the first time and proposes the design idea of a seven-layer model, namely the network, metadata, feature classification, selection input, processing, selection, and output layers. Among them, the processing layer divides link prediction methods into similarity-based, probabilistic, likelihood, supervised learning, semi-supervised learning, unsupervised learning, and reinforcement learning methods. The input features, evaluation metrics, complex analysis, experimental comparisons, relative merits, common dataset and open-source implementations for each link prediction method are then discussed in detail. Through analysis and comparison, we found that the link prediction method based on graph structure features has better prediction performance. Finally, the future development direction of link prediction in complex networks is discussed.


Author(s):  
Ranjan Kumar Behera ◽  
Kshira Sagar Sahoo ◽  
Debadatt Naik ◽  
Santanu Kumar Rath ◽  
Bibhudatta Sahoo

Link prediction is an emerging research problem in social network analysis, where future possible links are predicted based on the structural or the content information associated with the network. In this paper, various machine learning (ML) techniques have been utilized for predicting the future possible links based on the features extracted from the topological structure. Moreover, feature sets have been prepared by measuring different similarity metrics between all pair of nodes between which no link exists. For predicting the future possible links various supervised ML algorithms like K-NN, MLP, bagging, SVM, decision tree have been implemented. The feature set for each instance in the dataset has been prepared by measuring the similarity index between the non-existence links. The model has been trained to identify the new links which are likely to appear in the future but currently do not exist in the network. Further, the proposed model is validated through various performance metrics.


Entropy ◽  
2021 ◽  
Vol 23 (6) ◽  
pp. 664
Author(s):  
Nikos Kanakaris ◽  
Nikolaos Giarelis ◽  
Ilias Siachos ◽  
Nikos Karacapilidis

We consider the prediction of future research collaborations as a link prediction problem applied on a scientific knowledge graph. To the best of our knowledge, this is the first work on the prediction of future research collaborations that combines structural and textual information of a scientific knowledge graph through a purposeful integration of graph algorithms and natural language processing techniques. Our work: (i) investigates whether the integration of unstructured textual data into a single knowledge graph affects the performance of a link prediction model, (ii) studies the effect of previously proposed graph kernels based approaches on the performance of an ML model, as far as the link prediction problem is concerned, and (iii) proposes a three-phase pipeline that enables the exploitation of structural and textual information, as well as of pre-trained word embeddings. We benchmark the proposed approach against classical link prediction algorithms using accuracy, recall, and precision as our performance metrics. Finally, we empirically test our approach through various feature combinations with respect to the link prediction problem. Our experimentations with the new COVID-19 Open Research Dataset demonstrate a significant improvement of the abovementioned performance metrics in the prediction of future research collaborations.


Author(s):  
Givanna H Putri ◽  
Irena Koprinska ◽  
Thomas M Ashhurst ◽  
Nicholas J C King ◽  
Mark N Read

Abstract Motivation Many ‘automated gating’ algorithms now exist to cluster cytometry and single-cell sequencing data into discrete populations. Comparative algorithm evaluations on benchmark datasets rely either on a single performance metric, or a few metrics considered independently of one another. However, single metrics emphasize different aspects of clustering performance and do not rank clustering solutions in the same order. This underlies the lack of consensus between comparative studies regarding optimal clustering algorithms and undermines the translatability of results onto other non-benchmark datasets. Results We propose the Pareto fronts framework as an integrative evaluation protocol, wherein individual metrics are instead leveraged as complementary perspectives. Judged superior are algorithms that provide the best trade-off between the multiple metrics considered simultaneously. This yields a more comprehensive and complete view of clustering performance. Moreover, by broadly and systematically sampling algorithm parameter values using the Latin Hypercube sampling method, our evaluation protocol minimizes (un)fortunate parameter value selections as confounding factors. Furthermore, it reveals how meticulously each algorithm must be tuned in order to obtain good results, vital knowledge for users with novel data. We exemplify the protocol by conducting a comparative study between three clustering algorithms (ChronoClust, FlowSOM and Phenograph) using four common performance metrics applied across four cytometry benchmark datasets. To our knowledge, this is the first time Pareto fronts have been used to evaluate the performance of clustering algorithms in any application domain. Availability and implementation Implementation of our Pareto front methodology and all scripts and datasets to reproduce this article are available at https://github.com/ghar1821/ParetoBench. Supplementary information Supplementary data are available at Bioinformatics online.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Seyed Hossein Jafari ◽  
Amir Mahdi Abdolhosseini-Qomi ◽  
Masoud Asadpour ◽  
Maseud Rahgozar ◽  
Naser Yazdani

AbstractThe entities of real-world networks are connected via different types of connections (i.e., layers). The task of link prediction in multiplex networks is about finding missing connections based on both intra-layer and inter-layer correlations. Our observations confirm that in a wide range of real-world multiplex networks, from social to biological and technological, a positive correlation exists between connection probability in one layer and similarity in other layers. Accordingly, a similarity-based automatic general-purpose multiplex link prediction method—SimBins—is devised that quantifies the amount of connection uncertainty based on observed inter-layer correlations in a multiplex network. Moreover, SimBins enhances the prediction quality in the target layer by incorporating the effect of link overlap across layers. Applying SimBins to various datasets from diverse domains, our findings indicate that SimBins outperforms the compared methods (both baseline and state-of-the-art methods) in most instances when predicting links. Furthermore, it is discussed that SimBins imposes minor computational overhead to the base similarity measures making it a potentially fast method, suitable for large-scale multiplex networks.


2021 ◽  
Author(s):  
Mohamed G. El-Shafiey ◽  
Ahmed Hagag ◽  
El-Sayed A. El-Dahshan ◽  
Manal A. Ismail

F1000Research ◽  
2019 ◽  
Vol 8 ◽  
pp. 1459 ◽  
Author(s):  
Lukas M. Weber ◽  
Charlotte Soneson

Benchmarking is a crucial step during computational analysis and method development. Recently, a number of new methods have been developed for analyzing high-dimensional cytometry data. However, it can be difficult for analysts and developers to find and access well-characterized benchmark datasets. Here, we present HDCytoData, a Bioconductor package providing streamlined access to several publicly available high-dimensional cytometry benchmark datasets. The package is designed to be extensible, allowing new datasets to be contributed by ourselves or other researchers in the future. Currently, the package includes a set of experimental and semi-simulated datasets, which have been used in our previous work to evaluate methods for clustering and differential analyses. Datasets are formatted into standard SummarizedExperiment and flowSet Bioconductor object formats, which include complete metadata within the objects. Access is provided through Bioconductor's ExperimentHub interface. The package is freely available from http://bioconductor.org/packages/HDCytoData.


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