Evidence map›Paper›PMID 40531831›Full record

ArticlePloS one2025

Machine learning driven dashboard for chronic myeloid leukemia prediction using protein sequences.

Waqar Ahmad, Abdul Raheem Shahzad, Muhammad Awais Amin, Waqas Haider Bangyal, Tahani Jaser Alahmadi, Saddam Hussain Khan

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Waqar AhmadDepartment of Computer and Information Sciences, Pakistan Institute of Engineering and Applied Sciences, Islamabad, Pakistan.ORCID 0009-0007-4238-0856
Abdul Raheem ShahzadCECOS University of IT and Emerging Sciences, Peshawar, Khyber Pakhtunkhwa (KPK), Pakistan.
Muhammad Awais AminDepartment of Computer and Information Sciences, Pakistan Institute of Engineering and Applied Sciences, Islamabad, Pakistan.ORCID 0009-0001-4445-7606
Waqas Haider BangyalDepartment of Computer Science, Kohsar University Murree, Punjab, Pakistan.
Tahani Jaser AlahmadiDepartment of Information Systems, College of Computer and Information Sciences, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.ORCID 0000-0002-0067-692X
Saddam Hussain KhanArtificial Intelligence Lab, Department of Computer Systems Engineering, University of Engineering and Applied Sciences (UEAS), Swat, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prevalence of Leukaemia, a malignant blood cancer that originates from hematopoietic progenitor cells, is increasing in Southeast Asia, with a worrisome fatality rate of 54%. Predicting outcomes in the early stages is vital for improving the chances of patient recovery. The aim of this research is to enhance early-stage prediction systems in a substantial manner. Using Machine Learning and Data Science, we exploit protein sequential data from commonly altered genes including BCL2, HSP90, PARP, and RB to make predictions for Chronic Myeloid Leukaemia (CML). The methodology we implement is based on the utilisation of reliable methods for extracting features, namely Di-peptide Composition (DPC), Amino Acid Composition (AAC), and Pseudo amino acid composition (Pse-AAC). We also take into consideration the identification and handling of outliers, as well as the validation of feature selection using the Pearson Correlation Coefficient (PCA). Data augmentation guarantees a comprehensive dataset for analysis. By utilising several Machine Learning models such as Support Vector Machine (SVM), XGBoost, Random Forest (RF), K Nearest Neighbour (KNN), Decision Tree (DT), and Logistic Regression (LR), we have achieved accuracy rates ranging from 66% to 94%. These classifiers are thoroughly evaluated utilising performance criteria such as accuracy, sensitivity, specificity, F1-score, and the confusion matrix.The solution we suggest is a user-friendly online application dashboard that can be used for early detection of CML. This tool has significant implications for practitioners and may be used in healthcare institutions and hospitals.

Indexed as

Leukemia, Myelogenous, Chronic, BCR-ABL PositiveMachine LearningAmino Acid SequenceHumansProto-Oncogene Proteins c-bcl-2Support Vector MachineProto-Oncogene Proteins c-bcl-2

Identifiers

PMID40531831
PMCPMC12176232

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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.