Evidence map›Paper›PMID 38972881›Full record

ArticleScientific reports2024

Improving prediction of blood cancer using leukemia microarray gene data and Chi2 features with weighted convolutional neural network.

Ebtisam Abdullah Alabdulqader, Aisha Ahmed Alarfaj, Muhammad Umer, Ala' Abdulmajid Eshmawi, Shtwai Alsubai, Tai-Hoon Kim, Imran Ashraf

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In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Review
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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

7 authors.

Ebtisam Abdullah AlabdulqaderDepartment of Information Technology, College of Computer and Information Sciences, King Saud University, P. O. Box 800, 11421, Riyadh, Saudi Arabia.
Aisha Ahmed AlarfajDepartment of Information Systems, College of Computer and Information Sciences, Princess Nourah bint Abdulrahman University, P.O. Box 84428, 11671, Riyadh, Saudi Arabia.
Muhammad Umer *Department of Computer Science and Information Technology, The Islamia University of Bahawalpur, Bahawalpur, 63100, Pakistan.
Ala' Abdulmajid EshmawiDepartment of Cybersecurity, College of Computer Science and Engineering, University of Jeddah, Jeddah, 23218, Saudi Arabia.
Shtwai Alsubai *Department of Computer Science, College of Computer Engineering and Sciences, Prince Sattam bin Abdulaziz University, P.O. Box 151, 11942, Al-Kharj, Saudi Arabia.
Tai-Hoon KimSchool of Electrical and Computer Engineering, Yeosu Campus, Chonnam National University, 50, Daehak-ro, Yeosu-si, 59626, Jeollanam-do, Republic of Korea. taihoonn@chonnam.ac.kr.
Imran AshrafDepartment of Information and Communication Engineering, Yeungnam University, Gyeongsan, 38541, Korea. imranashraf@ynu.ac.kr.

Funding

Princess Nourah bint Abdulrahman University Researchers Supporting Project PNURSP2024R348
6 · The paper itself

Abstract

Blood cancer has emerged as a growing concern over the past decade, necessitating early diagnosis for timely and effective treatment. The present diagnostic method, which involves a battery of tests and medical experts, is costly and time-consuming. For this reason, it is crucial to establish an automated diagnostic system for accurate predictions. A particular field of focus in medical research is the use of machine learning and leukemia microarray gene data for blood cancer diagnosis. Even with a great deal of research, more improvements are needed to reach the appropriate levels of accuracy and efficacy. This work presents a supervised machine-learning algorithm for blood cancer prediction. This work makes use of the 22,283-gene leukemia microarray gene data. Chi-squared (Chi2) feature selection methods and the synthetic minority oversampling technique (SMOTE)-Tomek resampling is used to overcome issues with imbalanced and high-dimensional datasets. To balance the dataset for each target class, SMOTE-Tomek creates synthetic data, and Chi2 chooses the most important features to train the learning models from 22,283 genes. A novel weighted convolutional neural network (CNN) model is proposed for classification, utilizing the support of three separate CNN models. To determine the importance of the proposed approach, extensive experiments are carried out on the datasets, including a performance comparison with the most advanced techniques. Weighted CNN demonstrates superior performance over other models when coupled with SMOTE-Tomek and Chi2 techniques, achieving a remarkable 99.9% accuracy. Results from k-fold cross-validation further affirm the supremacy of the proposed model.

Indexed as

LeukemiaNeural Networks, ComputerAlgorithmsGene Expression ProfilingHematologic NeoplasmsHumansMachine LearningOligonucleotide Array Sequence AnalysisSupervised Machine Learning

Identifiers

PMID38972881
PMCPMC11228030

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