Guardado en:
Detalles Bibliográficos
Autores principales: Moris, Eugenia, Costábile, Alicia, Rey, Sebastián, Ferreiro, Irene, Hurtado, Joaquín, Luciano, Lizandra Lissette, Villagrán, Matías, Vázquez, Aisha Espino, Ramos, Jomari, Monteiro, Isadora, de Santiago, María Victoria, Moreno, Pilar, Moratorio, Gonzalo, Orlando, José Ignacio
Formato: Preprint
Publicado: 2026
Materias:
Acceso en línea:https://arxiv.org/abs/2605.16008
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
_version_ 1866918504089780224
author Moris, Eugenia
Costábile, Alicia
Rey, Sebastián
Ferreiro, Irene
Hurtado, Joaquín
Luciano, Lizandra Lissette
Villagrán, Matías
Vázquez, Aisha Espino
Ramos, Jomari
Monteiro, Isadora
de Santiago, María Victoria
Moreno, Pilar
Moratorio, Gonzalo
Orlando, José Ignacio
author_facet Moris, Eugenia
Costábile, Alicia
Rey, Sebastián
Ferreiro, Irene
Hurtado, Joaquín
Luciano, Lizandra Lissette
Villagrán, Matías
Vázquez, Aisha Espino
Ramos, Jomari
Monteiro, Isadora
de Santiago, María Victoria
Moreno, Pilar
Moratorio, Gonzalo
Orlando, José Ignacio
contents Plaque assays remain the gold standard readout of virus infectivity; however, plaque counting from plate images is labor-intensive and prone to inter-operator variability. We present an end-to-end, computer-aided workflow for cytopathic effect-based virus titration directly from laboratory plaque assay images. The proposed approach combines two models derived from the Segment Anything Model (SAM): a SAM2-based well-segmentation module that localizes assay wells across heterogeneous imaging conditions, and a SAM-based plaque-segmentation model that detects and enumerates plaques within each well. The method was evaluated on a mixed dataset comprising private plaque assay images of Mayaro virus and Coxsackievirus B3, together with public Vaccinia virus images from the VACVPlaque dataset. The pipeline outputs per-well plaque counts, automatically computes plaque-forming units per milliliter (PFU/mL), and is integrated into a web-based platform that allows users to review results and organize experiments. On held-out plates (17 from MAYV/CVB3 and 22 from VACV), the workflow generalized across two plate formats (6-well and 12-well) and showed strong agreement with manual annotations (Pearson correlation coefficients of 0.92 for MAYV/CVB3 and 0.88 for VACV). Automated plaque counts were further compared with annotations from four independent experts, demonstrating high concordance. The proposed system will be open sourced and publicly released upon acceptance of this manuscript to enable reproducible, scalable, and audit-ready plaque assay analysis while substantially reducing manual annotation effort.
format Preprint
id arxiv_https___arxiv_org_abs_2605_16008
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle End-to-end plaque counting and virus titration from laboratory plate images with deep learning
Moris, Eugenia
Costábile, Alicia
Rey, Sebastián
Ferreiro, Irene
Hurtado, Joaquín
Luciano, Lizandra Lissette
Villagrán, Matías
Vázquez, Aisha Espino
Ramos, Jomari
Monteiro, Isadora
de Santiago, María Victoria
Moreno, Pilar
Moratorio, Gonzalo
Orlando, José Ignacio
Computer Vision and Pattern Recognition
Plaque assays remain the gold standard readout of virus infectivity; however, plaque counting from plate images is labor-intensive and prone to inter-operator variability. We present an end-to-end, computer-aided workflow for cytopathic effect-based virus titration directly from laboratory plaque assay images. The proposed approach combines two models derived from the Segment Anything Model (SAM): a SAM2-based well-segmentation module that localizes assay wells across heterogeneous imaging conditions, and a SAM-based plaque-segmentation model that detects and enumerates plaques within each well. The method was evaluated on a mixed dataset comprising private plaque assay images of Mayaro virus and Coxsackievirus B3, together with public Vaccinia virus images from the VACVPlaque dataset. The pipeline outputs per-well plaque counts, automatically computes plaque-forming units per milliliter (PFU/mL), and is integrated into a web-based platform that allows users to review results and organize experiments. On held-out plates (17 from MAYV/CVB3 and 22 from VACV), the workflow generalized across two plate formats (6-well and 12-well) and showed strong agreement with manual annotations (Pearson correlation coefficients of 0.92 for MAYV/CVB3 and 0.88 for VACV). Automated plaque counts were further compared with annotations from four independent experts, demonstrating high concordance. The proposed system will be open sourced and publicly released upon acceptance of this manuscript to enable reproducible, scalable, and audit-ready plaque assay analysis while substantially reducing manual annotation effort.
title End-to-end plaque counting and virus titration from laboratory plate images with deep learning
topic Computer Vision and Pattern Recognition
url https://arxiv.org/abs/2605.16008