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M. Aktaruzzaman Opu
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Computer Vision / AI ResearchYear 2026Undergraduate 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
Zero-Label Microscopy Anomaly Detection

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.

Technology Stack

PyTorch 2.2Python 3.12DINOv2SQAFormerCAE-IFOpenCVLIVECell Dataset