2 · Vision models
Subtitles
- Task-specific models to foundation models
- DINO, DINOv2, and UNI
- Linear probes versus fine-tuning
- CLIP and BiomedCLIP
- Retrieval versus report generation
- LLaVA and LLaVA-Med
- Biomedical validation
Milestones
Possible exam questions
OPEN · Q1 — For DINO’s teacher EMA, compare \(m=0\), \(0.9\), \(0.999\), and \(1\). Why use a slowly changing teacher?
OPEN · Q2 — What could happen when DINOv2’s feature-spread regularization is removed, and what would you compare to test feature usefulness?
OPEN · Q3 — Encoder A scores 78% frozen / 86% fine-tuned; B scores 84% / 85%. Which wins in each setting, and what remains unknown?
OPEN · Q4 — Can adding a third CLIP text prompt change “abnormal” from 0.90 despite unchanged similarity? Is 0.90 a disease probability?
OPEN · Q5 — Two images in a CLIP batch have identical paired text. Why can’t each assign all probability to its own copy, and how could you fix it?
OPEN · Q6 — Can a frozen CLIP image vector be fed directly into a frozen text-only LLM just because their dimensions match? What training is missing?
OPEN · Q7 — For binary image quality control, choose between a frozen encoder + small head and an instruction-tuned VLM. What else would you measure?
RECALL · Q8 — Why use different augmented views of an image in visual self-supervision?
RECALL · Q9 — What is the purpose of a contrastive image–text objective?
RECALL · Q10 — What distinguishes image-to-report retrieval from report generation?
RECALL · Q11 — For fixed image features \(z=f_\theta(x)\), which parameters does a linear probe fit?
RECALL · Q12 — What makes validation external rather than an internal held-out test?