Evidence map›Paper›PMID 41940101›Full record

ArticleFrontiers in artificial intelligence2026

Using transfer learning approaches to predict RNA-Seq gene expression data for cancer classification.

Waqas Haider Bangyal, Adnan Ashraf, Zia Ul-Qayyum, Meshari Alazmi, Asma Abdullah Alfayez

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Article in Frontiers in artificial intelligence, 2026. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Waqas Haider BangyalDepartment of Computer Science, Kohsar University, Murree, Pakistan.
Adnan AshrafDepartment of Computer Science, Government College Women University Sialkot, Sialkot, Pakistan.
Zia Ul-QayyumDepartment of Computer Science, FAST - National University of Computer & Emerging Sciences, Islamabad, Pakistan.
Meshari AlazmiCollege of Computer Science and Engineering, University of Ha'il, Ha'il, Saudi Arabia.
Asma Abdullah AlfayezKing Abdullah International Medical Research Center, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a great need to categorize cancer types for early cancer detection and treatment. RNA-Seq data is essential for getting insight into the differentially expressed genes. Due to its high dimensionality and complexity, performing an analysis on RNA-Seq data is quite challenging. In the past, RNA-Seq data were analyzed for a single cancer type as a two-class problem (either positive or negative) and did not contain information from other classes of cancer types. To classify different cancer types and discover the most promising genes, RNA-Seq data for different types of cancer should be examined. Multiple repositories offer RNA-Seq-based cancer types data. The present study incorporates a dataset from the Mendeley repository for classification. RNA-Seq values are then converted to their respective 2D images using some transformations. The classification problem is handled by five Transfer Learning (TL) algorithms (VGG16, VGG19, Resnet50, Resnet101, and Resnet152). Four different splitting strategies are applied for each classifier presented in the results and discussion section. A comparative analysis is also carried out with and without data augmentation. Results show that classifiers perform best at a split of 70-30. VGG16 attained the best position on overall results by achieving an accuracy of 95%. Hence, VGG16 is the leading TL algorithm for classification among all the accessible models and is not difficult to execute and easy to comprehend.

Indexed as

cancergene expression dataResNetRNA-Seqtransfer learning

Identifiers

PMID41940101
PMCPMC13044096

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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.