Evidence map›Paper›PMID 42151364›Full record

ArticleScientific reports2026

Automated karyotyping and structural anomaly detection through a hybrid multi-stage deep learning framework integrating chromosome detection, pairwise classification, and autoencoder-based analysis.

Carolina Rosas-Alatriste, Noé Oswaldo Rodríguez-Rodríguez, Amadeo José Argüelles-Cruz, Alejandro Rosas-Cabral, Cornelio Yáñez-Márquez, Antonio Alarcón-Paredes

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Article in Scientific reports, 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Carolina Rosas-AlatristeInstituto Politécnico Nacional (IPN), Centro de Investigación en Computación (CIC), Ciudad de México, 07738, México.
Noé Oswaldo Rodríguez-RodríguezInstituto Politécnico Nacional (IPN), Centro de Investigación en Computación (CIC), Ciudad de México, 07738, México.
Amadeo José Argüelles-CruzInstituto Politécnico Nacional (IPN), Centro de Investigación en Computación (CIC), Ciudad de México, 07738, México.
Alejandro Rosas-CabralUniversidad Autónoma de Aguascalientes (UAA), Departamento de Medicina, Aguascalientes, 20100, México.
Cornelio Yáñez-MárquezInstituto Politécnico Nacional (IPN), Centro de Investigación en Computación (CIC), Ciudad de México, 07738, México.
Antonio Alarcón-ParedesInstituto Politécnico Nacional (IPN), Centro de Investigación en Computación (CIC), Ciudad de México, 07738, México. aalarcon@cic.ipn.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Manual karyotype analysis remains a labor-intensive and expertise-dependent process that requires visual interpretation of chromosome banding patterns under the microscope. Although recent studies have applied machine learning to isolated stages of chromosome detection, segmentation, or classification, few approaches address the complete cytogenetic workflow in a clinically aligned manner. This work proposes a stability-aware, multi-stage deep learning framework for semi-automated karyotype generation and chromosomal anomaly screening. The pipeline integrates: (i) an overlapped-aware quality-control gate to exclude morphologically unreliable metaphases; (ii) YOLOv8-based single-chromosome detection; (iii) homologous-pair assignment using both a unified YOLOv8 route and a hybrid YOLOv8 + fine-tuned ResNet-50 configuration across 24 chromosome classes; (iv) automatic karyotype assembly; and (v) unsupervised structural anomaly screening via a convolutional autoencoder trained exclusively on normal chromosomes. Experimental validation demonstrated 98.03% detection accuracy (mAP@0.5 = 0.985) and 94.01% validation accuracy for homologous-pair classification. Under sequential modeling, the propagated end-to-end numerical accuracy reached 92.21% for the hybrid configuration and 94.01% for the unified YOLOv8 configuration. The autoencoder exhibited clear separation between normal and structurally anomalous reconstruction-error distributions, enabling effective unsupervised screening without requiring extensive labeled pathological datasets. By explicitly modeling cumulative inter-stage dependency and enforcing morphological integrity through an upstream overlapped filter, the proposed framework provides a clinically interpretable and operationally coherent assistant system. The results demonstrate that stability-aware pipeline design can support both numerical and structural anomaly detection while reducing manual workload and preserving diagnostic transparency.

Indexed as

Deep LearningKaryotypingAutoencoderHumansAutoencoderChromosome detectionComputer visionCytogeneticsDeep learningKaryotype automationStructural anomaly

Identifiers

PMID42151364
PMCPMC13376932

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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.