Publication:
Machine learning-augmented lateral flow assays for point-of-care infectious disease diagnostics

dc.contributor.coauthorMorales-Narvaez, Eden
dc.contributor.coauthorYetisen, Ali K.
dc.contributor.departmentGraduate School of Sciences and Engineering
dc.contributor.departmentDepartment of Mechanical Engineering
dc.contributor.departmentSchool of Medicine
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentKUIS AI (Koç University & İş Bank Artificial Intelligence Center)
dc.contributor.departmentKUAR (KU Arçelik Research Center for Creative Industries)
dc.contributor.kuauthorParmaksızoğlu, Çağla
dc.contributor.kuauthorÇakıroğlu, Işıl
dc.contributor.kuauthorAtçeken, Nazente
dc.contributor.kuauthorTaşoğlu, Savaş
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF SCIENCES AND ENGINEERING
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2026-07-02T07:30:45Z
dc.date.issued2026
dc.description.abstractLateral flow assays (LFAs) are among the most widely used point-of-care (PoC) diagnostic platforms for infectious diseases due to their rapid operation, low cost, and user-friendly architecture. However, conventional LFAs remain limited by analytical sensitivity, qualitative or semi-quantitative outputs, and reliance on subjective visual interpretation. Recent innovations in nanomaterial engineering, signal amplification strategies, and multiplex assay design have significantly improved detection performance across viral, bacterial, and other pathogens. Advanced labels, CRISPR-assisted amplification, and dual-mode sensing formats have expanded the analytical capabilities of LFAs beyond traditional colorimetric designs. Parallel to material and biochemical advancements, AI and machine learning (ML)-based image analysis have emerged as transformative tools for digital LFA interpretation. Smartphone-assisted readers and convolutional neural networks (CNNs) enable objective, quantitative signal extraction, reduce user-dependent variability, and improve detection of weak test lines. These approaches support standardized analysis and scalable disease surveillance. Despite these advances, challenges remain in sensitivity optimization, dataset quality, standardization, and regulatory alignment of ML-enabled diagnostic platforms. Future integration of AI-driven analytics with robust assay engineering is expected to redefine LFA platforms as digitally connected, quantitative, and clinically reliable PoC diagnostic systems.
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dc.description.indexedbyScopus
dc.description.indexedbyPubMed
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dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipS. T. acknowledges the TUBITAK 2232 International Fellowship for Outstanding Researchers Award (118C391), TUBITAK-1001 Scientific and Technological Research Projects (123S582, 123Z050, 225S122, 125Z215), Alexander von Humboldt Research Fellowship for Experienced Researchers, Marie Sk & lstrok;odowska-Curie Individual Fellowship (101003361), and Royal Academy Newton-Katip Celebi Transforming Systems Through Partnership Award (120N019) for the financial support of this research. N. A. acknowledges support by EMBO Scientific Exchange Grant (11627) and TUBITAK-2218 Domestic Postdoctoral Research Scholarship Project (122C195). Opinions, interpretations, conclusions, and recommendations are those of the author and are not necessarily endorsed by the TUB & Idot;TAK. This work was partially supported by the Science Academy's Young Scientist Awards Program (BAGEP), Outstanding Young Scientists Awards (GEBIP), Dr. Nejat Eczacibasi Medicine Incentive Award, IBG Science Medal from Izmir Biomedicine and Genome Center, ELGINKAN Foundation Technology Prize, TGC Sedat Simavi Health Sciences Award, Parlar Foundation Research Incentive Award, Parlar Foundation Technology Incentive Award, and Bilim Kahramanlari Dernegi The Young Scientist Award. This study was conducted using the service and infrastructure of Koc University Translational Medicine Research Center (KUTTAM). E. M.-N. acknowledges the support of the Direccion General de Asuntos del Personal Academico de la Universidad Nacional Autonoma de Mexico (grant PAPIIT-IT100124). E. M.-N. also acknowledges support from Fundacion Marcos Moshinsky UNAM (Catedra Moshinsky 2024) and SECIHTI (grant MADTEC-2025-M-137). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. For the figures, Biorender was used.
dc.description.versionPublished Version
dc.identifier.WoSQuartileQ1
dc.identifier.doi10.1039/d5lc01124h
dc.identifier.eissn1473-0189
dc.identifier.embargoNo
dc.identifier.endpage2414
dc.identifier.grantno118C391
dc.identifier.grantno123S582
dc.identifier.grantno123Z050
dc.identifier.grantno225S122
dc.identifier.grantno125Z215
dc.identifier.grantno122C195
dc.identifier.issn1473-0197
dc.identifier.issue8
dc.identifier.pubmed41879655
dc.identifier.scopus2-s2.0-105036566808
dc.identifier.startpage2394
dc.identifier.urihttps://doi.org/10.1039/d5lc01124h
dc.identifier.urihttps://hdl.handle.net/20.500.14288/33060
dc.identifier.volume26
dc.identifier.wos001722650400001
dc.keywordsLateral flow assays
dc.keywordsArtificial intelligence
dc.keywordsPoint-of-care diagnostics
dc.languageeng
dc.publisherRoyal Society of Chemistry
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofLab on a Chip
dc.relation.openaccessN/A
dc.rightsN/A
dc.rights.uriN/A
dc.subjectBiochemical research methods
dc.subjectChemistry, multidisciplinary
dc.subjectChemistry, analytical
dc.subjectNanoscience and nanotechnology
dc.subjectInstruments and instrumentation
dc.titleMachine learning-augmented lateral flow assays for point-of-care infectious disease diagnostics
dc.typeReview
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