Evidence map›Paper›PMID 39911161›Full record

ArticleFrontiers in computational neuroscience2024

Automated karyogram analysis for early detection of genetic and neurodegenerative disorders: a hybrid machine learning approach.

Sumaira Tabassum, M Jawad Khan, Javaid Iqbal, Asim Waris, M Adeel Ijaz

Abstract read
In one paragraph

Article in Frontiers in computational neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Article
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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

5 authors.

Sumaira TabassumDepartment of Robotics and Artificial Intelligence, School of Mechanical and Manufacturing Engineering, National University of Sciences and Technology, Islamabad, Pakistan.
M Jawad KhanDepartment of Robotics and Artificial Intelligence, School of Mechanical and Manufacturing Engineering, National University of Sciences and Technology, Islamabad, Pakistan.
Javaid IqbalDepartment of Robotics and Artificial Intelligence, School of Mechanical and Manufacturing Engineering, National University of Sciences and Technology, Islamabad, Pakistan.
Asim WarisDepartment of Robotics and Artificial Intelligence, School of Mechanical and Manufacturing Engineering, National University of Sciences and Technology, Islamabad, Pakistan.
M Adeel IjazDepartment of Robotics and Artificial Intelligence, School of Mechanical and Manufacturing Engineering, National University of Sciences and Technology, Islamabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anomalous chromosomes are the cause of genetic diseases such as cancer, Alzheimer's, Parkinson's, epilepsy, and autism. Karyotype analysis is the standard procedure for diagnosing genetic disorders. Identifying anomalies is often costly, time-consuming, heavily reliant on expert interpretation, and requires considerable manual effort. Efforts are being made to automate karyogram analysis. However, the unavailability of large datasets, particularly those including samples with chromosomal abnormalities, presents a significant challenge. The development of automated models requires extensive labeled and incredibly abnormal data to accurately identify and analyze abnormalities, which are difficult to obtain in sufficient quantities. Although the deep learning-based architecture has yielded state-of-the-art performance in medical image anomaly detection, it cannot be generalized well because of the lack of anomalous datasets. This study introduces a novel hybrid approach that combines unsupervised and supervised learning techniques to overcome the challenges of limited labeled data and scalability in chromosomal analysis. An Autoencoder-based system is initially trained with unlabeled data to identify chromosome patterns. It is fine-tuned on labeled data, followed by a classification step using a Convolutional Neural Network (CNN). A unique dataset of 234,259 chromosome images, including the training, validation, and test sets, was used. Marking a significant achievement in the scale of chromosomal analysis. The proposed hybrid system accurately detects structural anomalies in individual chromosome images, achieving 99.3% accuracy in classifying normal and abnormal chromosomes. We also used a structural similarity index measure and template matching to identify the part of the abnormal chromosome that differed from the normal one. This automated model has the potential to significantly contribute to the early detection and diagnosis of chromosome-related disorders that affect both genetic health and neurological behavior.

Indexed as

chromosome anomaliescognitive sciencesgenetic diseasesmachine learningneurodevelopmental disordersneurological disordersneurological healthneuroscience

Identifiers

PMID39911161
PMCPMC11794836

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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.