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WBT-DC pipeline: a cross-cohort and cross-platform disease classification pipeline based on whole-blood transcriptomics

dc.contributor.authorLi, Mengzhen
dc.contributor.authorJin, Han
dc.contributor.authorMeng, Lingqi
dc.contributor.authorAltay, Ozlem
dc.contributor.authorYuksel, Bayram
dc.contributor.authorZhang, Cheng
dc.contributor.authorUhlen, Mathias
dc.contributor.authorTurkez, Hasan
dc.contributor.authorMardinoglu, Adil
dc.date.accessioned2026-11-05T11:07:54Z
dc.date.issued2026
dc.description.abstractBackground Machine-learning models based on tissue transcriptomic data are powerful tools for disease classification. However, their clinical adoption is limited by the invasive nature of tissue sampling. Furthermore, transcriptomic datasets are often affected by batch effects and gene-level noise, which compromise model generalizability across platforms and clinical cohorts. Methods We developed WBT-DC (Whole Blood Transcriptomics-based Disease Classification), a computational pipeline designed to overcome these challenges. WBT-DC integrates rank-based feature extraction to mitigate batch effects with an ensemble machine-learning framework that incorporates cross-validation and hyperparameter optimization. Its performance was systematically evaluated across five independent cohorts involving 2,164 participants and three disease contexts: Crohn's disease (CD), ulcerative colitis (UC), and amyotrophic lateral sclerosis (ALS). We tested the model's robustness across RNA-sequencing and microarray platforms. Additionally, an internal rheumatoid arthritis (RA) cohort (n = 165) was utilized for real-world prospective validation. Results WBT-DC demonstrated high accuracy, achieving ROC-AUC values of 0.90-0.94 in independent datasets when training and testing were conducted on the same platform. In cross-platform evaluations, the pipeline maintained robust performance with ROC-AUC values ranging from 0.71 to 0.84, consistently outperforming conventional gene expression-based models. In the RA validation cohort, WBT-DC achieved an ROC-AUC of 0.81, supporting its applicability in a real-world clinical setting. Conclusions WBT-DC provides a robust, non-invasive, and platform-agnostic framework for disease classification using whole-blood transcriptomics. By effectively addressing batch effects and platform variability, this pipeline offers a scalable solution for translating systems-level transcriptomic insights into applications. [GRAPHICS]
dc.description.issue1
dc.description.pages679
dc.description.sponsorshipOpen access funding provided by Royal Institute of Technology.
dc.description.volume24
dc.identifier.doi10.1186/s12967-026-08254-3
dc.identifier.issn1479-5876
dc.identifier.urihttps://doi.org/10.1186/s12967-026-08254-3
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/11494
dc.identifier.wosWOS:001766794800002
dc.language.isoen
dc.publisherBMC
dc.relation.fundingRoyal Institute of Technology(Spanish Government)
dc.relation.fundingRoyal Institute of Technology
dc.relation.hasversion10.1186/s12967-026-08254-3
dc.relation.ispartofJOURNAL OF TRANSLATIONAL MEDICINE
dc.subjectWhole blood transcriptomics
dc.subjectMachine learning
dc.subjectDisease prediction
dc.subjectPACKAGE
dc.subjectMedicine, Research & Experimental
dc.subjectResearch & Experimental Medicine
dc.titleWBT-DC pipeline: a cross-cohort and cross-platform disease classification pipeline based on whole-blood transcriptomics
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.issue1
oaire.citation.volume24
person.identifier.orcid0000-0002-3721-8586
person.identifier.ridAAQ-4905-2020
person.identifier.ridB-3262-2016
person.identifier.ridAAS-6360-2021
person.identifier.ridL-7906-2016

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