Evidence map›Paper›PMID 36624117›Full record

ArticleScientific reports2023

Constrained neuro fuzzy inference methodology for explainable personalised modelling with applications on gene expression data.

Balkaran Singh, Maryam Doborjeh, Zohreh Doborjeh, Sugam Budhraja, Samuel Tan, Alexander Sumich, Wilson Goh, Jimmy Lee, Edmund Lai, Nikola Kasabov

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Balkaran SinghKnowledge Engineering and Discovery Research Innovation (KEDRI), School of Engineering Computer and Mathematical Sciences, Auckland University of Technology, Auckland, New Zealand. balkaran.singh@aut.ac.nz.
Maryam DoborjehKnowledge Engineering and Discovery Research Innovation (KEDRI), School of Engineering Computer and Mathematical Sciences, Auckland University of Technology, Auckland, New Zealand. mgholami@aut.ac.nz.
Zohreh DoborjehSchool of Population Health, The University of Auckland, Auckland, New Zealand.
Sugam BudhrajaKnowledge Engineering and Discovery Research Innovation (KEDRI), School of Engineering Computer and Mathematical Sciences, Auckland University of Technology, Auckland, New Zealand.
Samuel TanLee Kong Chian School of Medicine, Nanyang Technological University (NTU), Singapore, Singapore.
Alexander SumichDepartment of Psychology, Nottingham Trent University, Nottingham, UK.
Wilson GohLee Kong Chian School of Medicine, Nanyang Technological University (NTU), Singapore, Singapore.
Jimmy LeeLee Kong Chian School of Medicine, Nanyang Technological University (NTU), Singapore, Singapore.
Edmund LaiKnowledge Engineering and Discovery Research Innovation (KEDRI), School of Engineering Computer and Mathematical Sciences, Auckland University of Technology, Auckland, New Zealand.
Nikola KasabovKnowledge Engineering and Discovery Research Innovation (KEDRI), School of Engineering Computer and Mathematical Sciences, Auckland University of Technology, Auckland, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interpretable machine learning models for gene expression datasets are important for understanding the decision-making process of a classifier and gaining insights on the underlying molecular processes of genetic conditions. Interpretable models can potentially support early diagnosis before full disease manifestation. This is particularly important yet, challenging for mental health. We hypothesise this is due to extreme heterogeneity issues which may be overcome and explained by personalised modelling techniques. Thus far, most machine learning methods applied to gene expression datasets, including deep neural networks, lack personalised interpretability. This paper proposes a new methodology named personalised constrained neuro fuzzy inference (PCNFI) for learning personalised rules from high dimensional datasets which are structurally and semantically interpretable. Case studies on two mental health related datasets (schizophrenia and bipolar disorders) have shown that the relatively short and simple personalised fuzzy rules provided enhanced interpretability as well as better classification performance compared to other commonly used machine learning methods. Performance test on a cancer dataset also showed that PCNFI matches previous benchmarks. Insights from our approach also indicated the importance of two genes (ATRX and TSPAN2) as possible biomarkers for early differentiation of ultra-high risk, bipolar and healthy individuals. These genes are linked to cognitive ability and impulsive behaviour. Our findings suggest a significant starting point for further research into the biological role of cognitive and impulsivity-related differences. With potential applications across bio-medical research, the proposed PCNFI method is promising for diagnosis, prognosis, and the design of personalised treatment plans for better outcomes in the future.

Indexed as

Bipolar DisorderFuzzy LogicAlgorithmsEarly Detection of CancerGene ExpressionHumansNeural Networks, Computer

Identifiers

PMID36624117
PMCPMC9829920

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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.