
A scalable, AI-driven platform for high-throughput biological imaging. Automated, reproducible, interpretable - from multi-well plates to actionable data.
20+
Morphological Endpoints
10
Organ Segmentations
2
Validated Modules
Fast
High-Throughput Ready
PixelVision is a scalable, AI-driven image analysis workbench designed to support high-throughput biological imaging data across multiple platforms, species, and experimental designs. It is particularly optimized for large-scale multi-well plate screening, enabling automated, reproducible phenotypic analysis across high-content, high-throughput studies. It serves as a unifying framework for organizing, visualizing, analyzing, and interpreting complex imaging data, bridging the gap between raw images and actionable biological insights.
A unified framework built to scale from a single experiment to enterprise-level screening campaigns.
Automated phenotypic analysis across thousands of wells with consistent, reproducible scoring.
Deep learning models detect abnormalities, mortality, and structural changes at unprecedented scale.
Precise organ- and cell-level quantification across multiple biological systems and imaging modalities.
Human-in-the-loop validation with image quality scoring, best-image selection, and override tools.
Unified experiment comparison with rich metadata linking dose, timepoint, and treatment conditions.
Extend automated image analysis to MPS and organ-on-a-chip platforms - bringing the same reproducible, high-throughput scoring to complex in vitro models.
Estimate BMD from dose-dependent morphological changes with built-in statistical workflows (coming soon).
Modules are the core functional building blocks of PixelVision. Each module is a self-contained, task-specific analysis pipeline designed to support a particular imaging platform, biological system, or experimental workflow.
The modules currently available are supported, production-ready implementations. However, PixelVision is inherently extensible:
Currently, PixelVision includes two supported modules, all operating within a unified framework that ensures consistent data handling, visualization, and outputs while allowing the platform to scale and evolve with new assays, species, and imaging technologies.
Automates the full zebrafish imaging pipeline – from raw multi-well plate images to validated phenotypic calls – enabling large-scale developmental toxicology studies with speed and precision.
FINS detects 20+ endpoints including axis curvature, scoliosis, tail bending, fin absence, trunk abnormalities, craniofacial defects, notochord defects, yolk sac edema, pericardial edema, pigmentation changes, and otolith defects in 5dpf Danio rerio larvae.
FINS segments 10 regions: eye, brain, otolith, swim bladder, notochord, yolk, pericardium, craniofacial region, otic vesicles, and pigment – with quantitative area and morphology measurements per organ.
FINS processes dorsal, lateral, and additional views per well. AI-driven QC scoring ranks image quality and auto-selects the best image before running morphology analysis.
Yes. Models are trained on large expert-annotated Danio rerio datasets and validated in peer-reviewed publications on PFAS developmental toxicity in SLAS Technology and Aquatic Toxicology.
CellVision brings intelligent morphological assessment to cell culture systems. Regional prediction maps reveal sub-well patterns invisible to manual review, enabling high-content screening at scale.
CellVision classifies wells into three categories: Normal, Stressed, and Abnormal — providing a nuanced readout beyond simple live/dead scoring.
Each well image is divided into a grid of sub-regions, each independently scored to create a spatial heatmap revealing edge effects or compound gradients invisible in well-level averages.
Yes. CellVision works with both 2D monolayer and 3D systems including spheroids and organoids, making it suitable for physiologically relevant in vitro models.
CellVision operates within the PixelVision framework, ingesting images from high-content imaging platforms. Results integrate with the platform’s QC, metadata, and BMD calculation tools (coming soon).
SpheroidVision enables automated, high-throughput analysis of 2D and 3D spheroids and organoids, capturing complex morphology, growth dynamics, and treatment responses with precision and scalability.
SpheroidVision supports both 2D and 3D culture systems, including tumor spheroids, organoids, and co-culture models, enabling analysis of physiologically relevant in vitro systems.
SpheroidVision delivers multi-scale morphological quantification, capturing features such as size, shape, and heterogeneity at both the whole-spheroid and individual cell levels.
Yes. SpheroidVision supports longitudinal analysis of spheroid growth, enabling time-resolved tracking of expansion, shrinkage, and treatment response across time-lapse experiments.
Yes. The platform supports both brightfield and fluorescence imaging, enabling multi-channel analysis such as tumor labeling, viability markers, and co-culture systems.
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Oktay A, McAfee A, Green A, Howard B, Truong L, Tanguay R, Shah R & Tandon A. (2025). “FINS: An Interactive Platform for Automated Zebrafish Image Analysis and Morphological Screening.” Submitted to SLAS Technology.