yayamomt/medgemma-4b-it-bbbc006-nuclei-count-lora

MedGemma Vision Fine-Tuning

<img src="https://raw.githubusercontent.com/unslothai/unsloth/main/images/made%20with%20unsloth.png" width="200" style="display: block; margin: 20px auto;" >

This model is a fine-tuned version of unsloth/medgemma-4b-it-bnb-4bit. It has been trained using TRL.

Model documentation: MedGemma

Base model: unsloth/medgemma-4b-it-bnb-4bit

Github repo: yahyamomtaz/medgemma-vision-fine-tuning

unsloth/medgemma-4b-it-bnb-4bit fine-tuned with LoRA on BBBC006 to estimate the number of Hoechst-stained U2OS nuclei in fluorescence microscopy images. MedGemma is a collection of Gemma 3 variants that are trained for performance on medical text and image comprehension.

<img src="medgemma.jpg" width="400">

The model takes an image and an instruction then returns JSON:

{"nuclei_count": 87}

Research use only. This is a proof-of-concept image-counting adapter, not a clinical, diagnostic, or production microscopy-analysis system.

Reuse

This repository is a LoRA adapter, not a standalone model. Load unsloth/medgemma-4b-it-bnb-4bit first, then attach this adapter with PEFT. The published README.md includes a complete copyable inference example. Use the exact training prompt and preprocess 16-bit TIFFs as during training: per-image 1st--99.5th percentile scaling to 8-bit grayscale, followed by RGB conversion. The expected output is JSON, for example {"nuclei_count": 87}.

Training data

The labeled dataset was created from BBBC006 v1, which contains Hoechst-stained U2OS microscopy images from 384 wells, with two fields of view per well. This adapter uses the z=16, w1 (Hoechst/DAPI) TIFF images.

Targets are the BBBC006 Image_Count_Nuclei values. BBBC006 documents these as automated counts generated from the optimal-focus z=16 plane using CellProfiler's IdentifyPrimaryObjects. These are automated reference counts, not independent manual annotations.

Data processing

1. 1.Match z=16 TIFF files to BBBC006 count records using the stable well and site identifiers. The UUID suffixes differ between the image archive and count CSV.
2. 2.Retain only w1 Hoechst/DAPI images and exclude the w2 phalloidin channel.
3. 3.Scale each 16-bit grayscale TIFF independently using its 1st and 99.5th intensity percentiles, convert it to 8-bit grayscale, and then convert it to RGB.
4. 4.Split the data by well using seed 42 and an 80/20 ratio. Both sites from each well remain in the same split.
5. 5.Train the model to answer the fixed instruction with {"nuclei_count": <integer>}.

The training implementation is scripts/fine_tune_medgemma_vision.py in the source project.

Training

This model was trained with SFT.

The run uses load_best_model_at_end, selecting epoch 4 by validation loss (eval_loss=0.2677).

Framework versions

• —PEFT 0.20.0
• —TRL: 0.24.0
• —Transformers: 5.5.0
• —Pytorch: 2.6.0+cu124
• —Datasets: 4.3.0
• —Tokenizers: 0.22.2

Result

The final adapter and base model were evaluated on the same 154-image, 77-well held-out BBBC006 split. Both fields of view from a well are assigned to the same split. Both models used identical prompts, image preprocessing, and deterministic decoding.

The training-reference-mean baseline predicts 106.4967 nuclei for every image and has MAE 29.90 and RMSE 40.07 on the same split. The fine-tuned model's mean prediction is 97.25 versus a mean reference count of 98.91. This comparison shows that the adapter learned image-dependent counting within BBBC006; it is not an external benchmark comparison.

Evaluation output

The standalone evaluator generates full_eval_predictions.json in the adapter output directory. It includes:

• —aggregate MAE, RMSE, MAPE, and valid-output count;
• —every held-out image path and reference count;
• —the raw model response;
• —the parsed predicted_nuclei_count.

The complete 154-image results are at full_eval_predictions.json. The separate eval_predictions.json file contains only the deterministic 10-image post-training spot check.

Use case

Use this adapter for research experiments that investigate whether a vision-language model can estimate BBBC006 automated nucleus counts from optimal-focus z=16 Hoechst images. Outputs should be parsed as JSON and reviewed alongside the image.

It is not intended for cell segmentation, instance-level nucleus localization, clinical microscopy, general cell counting, or measurements without quality control.

Quick start

from transformers import pipeline

question = "If you had a time machine, but could only go to the past or the future once and never return, which would you choose and why?"
generator = pipeline("text-generation", model="None", device="cuda")
output = generator([{"role": "user", "content": question}], max_new_tokens=128, return_full_text=False)[0]
print(output["generated_text"])

License and attribution

The adapter is a derivative of MedGemma and is subject to the applicable Health AI Developer Foundations terms. Cite BBBC006 when using its images or labels, and verify all applicable terms before redistribution.

Citation

The model has been trained using TRL.

If you use this adapter, cite BBBC006.

@misc{vonwerra2022trl,
	title        = {{TRL: Transformer Reinforcement Learning}},
	author       = {Leandro von Werra and Younes Belkada and Lewis Tunstall and Edward Beeching and Tristan Thrush and Nathan Lambert and Shengyi Huang and Kashif Rasul and Quentin Gallou{\'e}dec},
	year         = 2020,
	journal      = {GitHub repository},
	publisher    = {GitHub},
	howpublished = {\url{https://github.com/huggingface/trl}}
}

@article{ljosa2012annotated,
  title={Annotated high-throughput microscopy image sets for validation},
  author={Ljosa, Vebjorn and others},
  journal={Nature Methods},
  year={2012}
}