# iMedImage Technical Report

arXiv: https://arxiv.org/abs/2503.21836 · HTML: https://mlsanity.com/paper/2503.21836/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 12 of its 22 references that are in the map.
- First posted on arXiv 27 Mar 2025.

## Builds on (most cited first, 12 of 12)

- [Attention Is All You Need](https://mlsanity.com/paper/1706.03762/) (2017)
- [Learning Transferable Visual Models From Natural Language Supervision](https://mlsanity.com/paper/2103.00020/) (2021)
- [U-Net: Convolutional Networks for Biomedical Image Segmentation](https://mlsanity.com/paper/1505.04597/) (2015)
- [Chain-of-Thought Prompting Elicits Reasoning in Large Language Models](https://mlsanity.com/paper/2201.11903/) (2022)
- [On the Opportunities and Risks of Foundation Models](https://mlsanity.com/paper/2108.07258/) (2021)
- [Outrageously Large Neural Networks: The Sparsely-Gated Mixture-of-Experts Layer](https://mlsanity.com/paper/1701.06538/) (2017)
- [A Survey on Deep Learning in Medical Image Analysis](https://mlsanity.com/paper/1702.05747/) (2017)
- [MedMNIST v2 -- A large-scale lightweight benchmark for 2D and 3D biomedical image classification](https://mlsanity.com/paper/2110.14795/) (2021)
- [Contrastive Learning of Medical Visual Representations from Paired Images and Text](https://mlsanity.com/paper/2010.00747/) (2020)
- [Big Self-Supervised Models Advance Medical Image Classification](https://mlsanity.com/paper/2101.05224/) (2021)
- [Med3D: Transfer Learning for 3D Medical Image Analysis](https://mlsanity.com/paper/1904.00625/) (2019)
- [Chromosomal Structural Abnormality Diagnosis by Homologous Similarity](https://mlsanity.com/paper/2407.08204/) (2024)

## Abstract (arXiv)

Background: Chromosome karyotype analysis is crucial for diagnosing hereditary diseases, yet detecting structural abnormalities remains challenging. While AI has shown promise in medical imaging, its effectiveness varies across modalities. Leveraging advances in Foundation Models that integrate multimodal medical imaging for robust feature extraction and accurate diagnosis, we developed iMedImage, an end-to-end model for general medical image recognition, demonstrating strong performance across multiple imaging tasks, including chromosome abnormality detection. Materials and Methods: We constructed a comprehensive medical image dataset encompassing multiple modalities from common medical domains, including chromosome, cell, pathology, ultrasound, X-ray, CT, and MRI images. Based on this dataset, we developed the iMedImage model, which incorporates the following key features: (1) a unified representation method for diverse modality inputs and medical imaging tasks; (2) multi-level (case-level, image-level, patch-level) image recognition capabilities enhanced by Chain of Thought (CoT) embedding and Mixture of Experts (MoE) strategies. Results: The test set comprised data from 12 institutions across six regions in China, covering three mainstream scanning devices, and included naturally distributed, unscreened abnormal cases. On this diverse dataset, the model achieved a fully automated chromosome analysis workflow, including segmentation, karyotyping, and abnormality detection, reaching a sensitivity of 92.75% and a specificity of 91.5%. Conclusion: We propose iMedImage, an end-to-end foundation model for medical image analysis, demonstrating its superior performance across various medical imaging tasks. iMedImage provides clinicians with a precise imaging analysis tool and contributes to improving diagnostic accuracy and disease screening.