Computer Vision / AI ResearchYear 2026•Undergraduate Thesis
Zero-Label Microscopy Anomaly Detection
Benchmarking CAE-IF, SQAFormer & DINOv2 for cell anomaly detection.
DomainComputer Vision / AI Research
Timeline2026
Technologies7 Stack Tools
StatusUndergraduate Thesis

The Problem
Pixel-reconstruction autoencoders fail on microscopy anomaly detection when corrupted images yield lower reconstruction error than sharp, high-contrast healthy cell membranes.
What It Does
- ✓Benchmarking 3 model paradigms (CAE-IF, SQAFormer, DINOv2 ViT embeddings) across 5,239 LIVECell frames
- ✓Empirical identification of catastrophic score sign inversion in reconstruction loss metrics
- ✓Feature extraction using self-supervised DINOv2 vision transformer backbones
- ✓Zero-shot metric evaluation including AUROC, AUPR, and Mahalanobis distance scoring
- ✓Anomaly visualization maps for cell image patches
How It Works & Architecture
PyTorch benchmarking pipeline. Cell frames pass through DINOv2 ViT backbones, and anomaly scoring is computed via latent feature space distances rather than pixel reconstruction error.
Technical Challenges
- !Handling high-dimensional embeddings across 8 distinct cell lines without supervision.
- !Analyzing why mean squared error favors smooth blurred artifacts over sharp cell textures.
What I Learned
- ★Pixel MSE reconstruction error is an unreliable metric for biological visual anomaly detection.
- ★Self-supervised vision foundation models capture structure far better than task-specific trained autoencoders.
On This Page
Technology Stack
PyTorch 2.2Python 3.12DINOv2SQAFormerCAE-IFOpenCVLIVECell Dataset