scholarly journals Evaluation of Gene Association Methods for Coexpression Network Construction and Biological Knowledge Discovery

PLoS ONE ◽  
2012 ◽  
Vol 7 (11) ◽  
pp. e50411 ◽  
Author(s):  
Sapna Kumari ◽  
Jeff Nie ◽  
Huann-Sheng Chen ◽  
Hao Ma ◽  
Ron Stewart ◽  
...  
2022 ◽  
Vol 7 (1) ◽  
Author(s):  
Alessandro Muscolino ◽  
Antonio Di Maria ◽  
Rosaria Valentina Rapicavoli ◽  
Salvatore Alaimo ◽  
Lorenzo Bellomo ◽  
...  

Abstract Background The rapidly increasing biological literature is a key resource to automatically extract and gain knowledge concerning biological elements and their relations. Knowledge Networks are helpful tools in the context of biological knowledge discovery and modeling. Results We introduce a novel system called NETME, which, starting from a set of full-texts obtained from PubMed, through an easy-to-use web interface, interactively extracts biological elements from ontological databases and then synthesizes a network inferring relations among such elements. The results clearly show that our tool is capable of inferring comprehensive and reliable biological networks.


PLoS ONE ◽  
2017 ◽  
Vol 12 (4) ◽  
pp. e0175104 ◽  
Author(s):  
Xingang Jia ◽  
Guanqun Zhu ◽  
Qiuhong Han ◽  
Zuhong Lu

Author(s):  
Lilit Nersisyan ◽  
Henry Löffler-Wirth ◽  
Arsen Arakelyan ◽  
Hans Binder

Genome-wide ‘omics'-assays provide a comprehensive view on the molecular landscapes of healthy and diseased cells. Bioinformatics traditionally pursues a ‘gene-centered' view by extracting lists of genes differentially expressed or methylated between healthy and diseased states. Biological knowledge mining is then performed by applying gene set techniques using libraries of functional gene sets obtained from independent studies. This analysis strategy neglects two facts: (i) that different disease states can be characterized by a series of functional modules of co-regulated genes and (ii) that the topology of the underlying regulatory networks can induce complex expression patterns that require analysis methods beyond traditional genes set techniques. The authors here provide a knowledge discovery method that overcomes these shortcomings. It combines machine learning using self-organizing maps with pathway flow analysis. It extracts and visualizes regulatory modes from molecular omics data, maps them onto selected pathways and estimates the impact of pathway-activity changes. The authors illustrate the performance of the gene set and pathway signal flow methods using expression data of oncogenic pathway activation experiments and of patient data on glioma, B-cell lymphoma and colorectal cancer.


2012 ◽  
Vol 20 (1) ◽  
pp. 1-2
Author(s):  
Mohammad Al Hasan ◽  
Jun Huan ◽  
Jake Chen ◽  
Mohammed J. Zaki

2017 ◽  
Vol 14 (1) ◽  
Author(s):  
Keywan Hassani-Pak ◽  
Christopher Rawlings

AbstractGenetics and “omics” studies designed to uncover genotype to phenotype relationships often identify large numbers of potential candidate genes, among which the causal genes are hidden. Scientists generally lack the time and technical expertise to review all relevant information available from the literature, from key model species and from a potentially wide range of related biological databases in a variety of data formats with variable quality and coverage. Computational tools are needed for the integration and evaluation of heterogeneous information in order to prioritise candidate genes and components of interaction networks that, if perturbed through potential interventions, have a positive impact on the biological outcome in the whole organism without producing negative side effects. Here we review several bioinformatics tools and databases that play an important role in biological knowledge discovery and candidate gene prioritization. We conclude with several key challenges that need to be addressed in order to facilitate biological knowledge discovery in the future.


Entropy ◽  
2020 ◽  
Vol 22 (7) ◽  
pp. 794
Author(s):  
Alessio Martino ◽  
Enrico De Santis ◽  
Alessandro Giuliani ◽  
Antonello Rizzi

Multiple kernel learning is a paradigm which employs a properly constructed chain of kernel functions able to simultaneously analyse different data or different representations of the same data. In this paper, we propose an hybrid classification system based on a linear combination of multiple kernels defined over multiple dissimilarity spaces. The core of the training procedure is the joint optimisation of kernel weights and representatives selection in the dissimilarity spaces. This equips the system with a two-fold knowledge discovery phase: by analysing the weights, it is possible to check which representations are more suitable for solving the classification problem, whereas the pivotal patterns selected as representatives can give further insights on the modelled system, possibly with the help of field-experts. The proposed classification system is tested on real proteomic data in order to predict proteins’ functional role starting from their folded structure: specifically, a set of eight representations are drawn from the graph-based protein folded description. The proposed multiple kernel-based system has also been benchmarked against a clustering-based classification system also able to exploit multiple dissimilarities simultaneously. Computational results show remarkable classification capabilities and the knowledge discovery analysis is in line with current biological knowledge, suggesting the reliability of the proposed system.


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