Add GliomaSAM3-MoE and SegMamba model weights
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- .gitattributes +9 -0
- README.md +97 -0
- gliomasam3_moe/checkpoints/ckpt_step2000.pt +3 -0
- gliomasam3_moe/checkpoints/ckpt_step2600.pt +3 -0
- gliomasam3_moe/checkpoints/ckpt_step3000.pt +3 -0
- gliomasam3_moe/configs/train.yaml +76 -0
- gliomasam3_moe/eval_results/table4_et_absent.json +43 -0
- gliomasam3_moe/eval_results/table7_boundary_dice.json +26 -0
- gliomasam3_moe/vis_res/README.md +206 -0
- gliomasam3_moe/vis_res/ampmix/Fig8_a_ampmix_BraTS-GLI-00005-000.pdf +3 -0
- gliomasam3_moe/vis_res/ampmix/Fig8_a_ampmix_BraTS-GLI-00005-000.png +3 -0
- gliomasam3_moe/vis_res/boundary/Fig3_a_boundary_BraTS-GLI-00005-000.pdf +3 -0
- gliomasam3_moe/vis_res/boundary/Fig3_a_boundary_BraTS-GLI-00005-000.png +3 -0
- gliomasam3_moe/vis_res/boundary/Fig3_b_boundary_BraTS-GLI-00017-000.pdf +3 -0
- gliomasam3_moe/vis_res/boundary/Fig3_b_boundary_BraTS-GLI-00017-000.png +3 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_a1_et_overview_BraTS-GLI-00005-000.pdf +0 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_a1_et_overview_BraTS-GLI-00005-000.png +3 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_a2_fragmentation_BraTS-GLI-00005-000.pdf +0 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_a2_fragmentation_BraTS-GLI-00005-000.png +3 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_a3_scale_BraTS-GLI-00005-000.pdf +0 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_a3_scale_BraTS-GLI-00005-000.png +3 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_b1_et_overview_BraTS-GLI-00006-000.pdf +3 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_b1_et_overview_BraTS-GLI-00006-000.png +3 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_b2_fragmentation_BraTS-GLI-00006-000.pdf +0 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_b2_fragmentation_BraTS-GLI-00006-000.png +3 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_b3_scale_BraTS-GLI-00006-000.pdf +0 -0
- gliomasam3_moe/vis_res/concept_tokens/Fig6_b3_scale_BraTS-GLI-00006-000.png +3 -0
- gliomasam3_moe/vis_res/dual_domain/Fig7_a_dual_domain_BraTS-GLI-00005-000.pdf +3 -0
- gliomasam3_moe/vis_res/dual_domain/Fig7_a_dual_domain_BraTS-GLI-00005-000.png +3 -0
- gliomasam3_moe/vis_res/dual_domain/Fig7_b_dual_domain_BraTS-GLI-00017-000.pdf +3 -0
- gliomasam3_moe/vis_res/dual_domain/Fig7_b_dual_domain_BraTS-GLI-00017-000.png +3 -0
- gliomasam3_moe/vis_res/et_absent/Fig2_a_et_absent_BraTS-GLI-00012-000.pdf +3 -0
- gliomasam3_moe/vis_res/et_absent/Fig2_a_et_absent_BraTS-GLI-00012-000.png +3 -0
- gliomasam3_moe/vis_res/failure/Fig9_a_failure_BraTS-GLI-00020-000.pdf +3 -0
- gliomasam3_moe/vis_res/failure/Fig9_a_failure_BraTS-GLI-00020-000.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/gt_ET.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/gt_TC.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/gt_WT.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/gt_overlay.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/input_FLAIR.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/input_T1.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/input_T1ce.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/input_T2.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/pred_gliomasam_step2000_ET.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/pred_gliomasam_step2000_TC.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/pred_gliomasam_step2000_WT.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/pred_gliomasam_step2000_overlay.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/pred_gliomasam_step2600_ET.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/pred_gliomasam_step2600_TC.png +3 -0
- gliomasam3_moe/vis_res/method_comparison/BraTS-GLI-00005-000/pred_gliomasam_step2600_WT.png +3 -0
.gitattributes
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# Video files - compressed
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# Video files - compressed
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*.mp4 filter=lfs diff=lfs merge=lfs -text
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*.webm filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/ampmix/Fig8_a_ampmix_BraTS-GLI-00005-000.pdf filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/boundary/Fig3_a_boundary_BraTS-GLI-00005-000.pdf filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/boundary/Fig3_b_boundary_BraTS-GLI-00017-000.pdf filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/concept_tokens/Fig6_b1_et_overview_BraTS-GLI-00006-000.pdf filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/dual_domain/Fig7_a_dual_domain_BraTS-GLI-00005-000.pdf filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/dual_domain/Fig7_b_dual_domain_BraTS-GLI-00017-000.pdf filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/et_absent/Fig2_a_et_absent_BraTS-GLI-00012-000.pdf filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/failure/Fig9_a_failure_BraTS-GLI-00020-000.pdf filter=lfs diff=lfs merge=lfs -text
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gliomasam3_moe/vis_res/qualitative/Fig1_qualitative_comparison.pdf filter=lfs diff=lfs merge=lfs -text
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README.md
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# SegMamba & GliomaSAM3-MoE Model Weights and Results
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This repository contains pre-trained model weights, evaluation results, and visualization outputs for brain tumor segmentation on BraTS 2023 dataset.
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## Repository Structure
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```
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├── gliomasam3_moe/
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│ ├── checkpoints/ # GliomaSAM3-MoE model weights
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│ │ ├── ckpt_step2000.pt
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│ │ ├── ckpt_step2600.pt
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│ │ └── ckpt_step3000.pt # Best checkpoint
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│ ├── configs/
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│ │ └── train.yaml # Training configuration
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│ ├── eval_results/
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│ │ ├── table4_et_absent.json # ET presence classification results
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│ │ └── table7_boundary_dice.json # Boundary-band Dice results
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│ └── vis_res/ # Visualization results
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│ ├── method_comparison/ # Side-by-side comparisons
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│ ├── boundary/ # Boundary analysis figures
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│ ├── moe_routing/ # MoE routing visualizations
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│ └── ...
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│
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├── segmamba/
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│ ├── checkpoints/ # SegMamba model weights
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│ │ ├── tmp_model_ep599_0.8295.pt
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│ │ └── tmp_model_ep799_0.8498.pt # Best checkpoint (Dice=0.8498)
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│ └── prediction_results/
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│ ├── segmamba_brats23_ep799/ # Prediction NIfTI files
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│ └── result_metrics/ # Evaluation metrics
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│
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└── README.md
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```
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## Model Performance
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### GliomaSAM3-MoE (ckpt_step3000)
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**Boundary-band Dice (3-voxel band):**
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| Region | Dice |
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|--------|------|
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| WT | 0.789 ± 0.057 |
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| TC | 0.766 ± 0.154 |
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| ET | 0.697 ± 0.161 |
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| **Mean** | **0.750** |
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**ET Presence Classification:**
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| Metric | Value |
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|--------|-------|
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| AUROC | 0.896 |
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| Accuracy | 0.795 |
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| Sensitivity | 0.792 |
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| Specificity | 1.000 |
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### SegMamba (ep799)
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- Mean Dice: 0.8498
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- Trained for 800 epochs on BraTS 2023
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## Usage
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### Loading GliomaSAM3-MoE
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```python
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import torch
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# Load checkpoint
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ckpt = torch.load("gliomasam3_moe/checkpoints/ckpt_step3000.pt", map_location="cpu")
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# Model state dict is in ckpt["model"]
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model.load_state_dict(ckpt["model"])
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```
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### Loading SegMamba
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```python
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import torch
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# Load checkpoint
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ckpt = torch.load("segmamba/checkpoints/tmp_model_ep799_0.8498.pt", map_location="cpu")
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# Model state dict
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model.load_state_dict(ckpt["model"])
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```
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## Data
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Models were trained and evaluated on BraTS 2023 GLI Challenge dataset (122 cases in processed subset).
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## Citation
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If you use these models, please cite the relevant papers.
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## License
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Please refer to the original model repositories for licensing information.
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gliomasam3_moe/checkpoints/ckpt_step2000.pt
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version https://git-lfs.github.com/spec/v1
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oid sha256:886d389ca84282d411b5a8643d578bc540ef32477c05b498a66d2ef8c62e6507
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size 1821693123
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gliomasam3_moe/checkpoints/ckpt_step2600.pt
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version https://git-lfs.github.com/spec/v1
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oid sha256:5886858a63de35d717697158e747060ca9df3104a2d92637cb040966a8af96e2
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size 1821693123
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gliomasam3_moe/checkpoints/ckpt_step3000.pt
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version https://git-lfs.github.com/spec/v1
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oid sha256:ffe568c3046807bb3b15bd36427ac935cd495acac15cd4937988b92f85cbab1a
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size 1821693123
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gliomasam3_moe/configs/train.yaml
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seed: 42
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device: "cuda"
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amp: true
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synthetic: false
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data:
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format: "segmamba_npz"
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root_dir: "/data/yty/brats23_segmamba_processed"
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modalities: ["t1n", "t1c", "t2f", "t2w"]
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seg_name: "seg"
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orientation: "RAS"
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do_spacing: false
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spacing: [1.0, 1.0, 1.0]
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crop_size: [128, 128, 128]
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num_samples: 1
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rand_scale_prob: 0.1
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rand_shift_prob: 0.1
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batch_size: 6
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synthetic_shape: [16, 128, 128]
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synthetic_cases: 16
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train_rate: 0.7
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val_rate: 0.1
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test_rate: 0.2
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segmamba_unpack: true
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model:
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patch_size: 14
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token_dim: 128
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depth: 3
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heads: 4
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mlp_ratio: 4.0
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slice_attn_k: 6
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slice_attn_random_dir: true
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spectral_bins: 24
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spectral_q: 3
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msda_scales: [3, 5, 7]
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moe_experts: 5
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moe_topk: 2
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decoder_hidden: 96
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prompt_mlp_hidden: 128
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use_sam3_backbone: true
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sam3_ckpt_path: "/data/yty/sam3/sam3.pt"
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sam3_freeze: true
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sam3_in_chans: 7
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sam3_input_mean: [0.5, 0.5, 0.5]
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sam3_input_std: [0.5, 0.5, 0.5]
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loss:
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dice_weight: 1.0
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bce_weight: 1.0
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et_focal_weight: 0.5
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focal_gamma: 2.0
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pres_weight: 0.1
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hier_weight: 0.1
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moe_weight: 0.01
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train:
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epochs: 300
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+
max_steps: 10000
|
| 60 |
+
lr: 0.0002
|
| 61 |
+
weight_decay: 0.00001
|
| 62 |
+
log_every: 20
|
| 63 |
+
save_every: 200
|
| 64 |
+
ckpt_dir: "./logs/segmamba/model"
|
| 65 |
+
fourier_mix_prob: 0.2
|
| 66 |
+
num_workers: 4
|
| 67 |
+
use_label_prompt: true
|
| 68 |
+
test_every_epochs: 5
|
| 69 |
+
test_max_cases: 0
|
| 70 |
+
|
| 71 |
+
infer:
|
| 72 |
+
roi_size: [128, 128, 128]
|
| 73 |
+
sw_batch_size: 1
|
| 74 |
+
overlap: 0.5
|
| 75 |
+
threshold: 0.5
|
| 76 |
+
et_cc_min_size: 50
|
gliomasam3_moe/eval_results/table4_et_absent.json
ADDED
|
@@ -0,0 +1,43 @@
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
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|
|
|
|
|
|
|
|
|
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|
|
|
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|
|
|
|
|
|
|
|
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|
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|
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|
|
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|
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|
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|
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|
|
|
|
|
|
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|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| 1 |
+
{
|
| 2 |
+
"et_absent_subset": {
|
| 3 |
+
"n": 2,
|
| 4 |
+
"fp_volume_mm3": {
|
| 5 |
+
"mean": 74.5,
|
| 6 |
+
"std": 74.5,
|
| 7 |
+
"min": 0.0,
|
| 8 |
+
"max": 149.0
|
| 9 |
+
},
|
| 10 |
+
"fp_components": {
|
| 11 |
+
"mean": 0.5,
|
| 12 |
+
"std": 0.5,
|
| 13 |
+
"min": 0,
|
| 14 |
+
"max": 1
|
| 15 |
+
}
|
| 16 |
+
},
|
| 17 |
+
"et_absent_cases": [
|
| 18 |
+
{
|
| 19 |
+
"case_id": "BraTS-GLI-00017-001",
|
| 20 |
+
"fp_volume_mm3": 149,
|
| 21 |
+
"fp_components": 1
|
| 22 |
+
},
|
| 23 |
+
{
|
| 24 |
+
"case_id": "BraTS-GLI-00048-001",
|
| 25 |
+
"fp_volume_mm3": 0,
|
| 26 |
+
"fp_components": 0
|
| 27 |
+
}
|
| 28 |
+
],
|
| 29 |
+
"classification": {
|
| 30 |
+
"n": 122,
|
| 31 |
+
"n_et_present": 120,
|
| 32 |
+
"n_et_absent": 2,
|
| 33 |
+
"auroc": 0.8958333333333333,
|
| 34 |
+
"optimal_threshold": 0.9947388768196106,
|
| 35 |
+
"accuracy_optimal": 0.7950819672131147,
|
| 36 |
+
"sensitivity_optimal": 0.7916666666666666,
|
| 37 |
+
"specificity_optimal": 1.0
|
| 38 |
+
},
|
| 39 |
+
"config": {
|
| 40 |
+
"min_size": 50,
|
| 41 |
+
"threshold": 0.5
|
| 42 |
+
}
|
| 43 |
+
}
|
gliomasam3_moe/eval_results/table7_boundary_dice.json
ADDED
|
@@ -0,0 +1,26 @@
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| 1 |
+
{
|
| 2 |
+
"stats": {
|
| 3 |
+
"WT": {
|
| 4 |
+
"mean": 0.7889820841743286,
|
| 5 |
+
"std": 0.05687755328186895,
|
| 6 |
+
"n": 122
|
| 7 |
+
},
|
| 8 |
+
"TC": {
|
| 9 |
+
"mean": 0.7656578316169296,
|
| 10 |
+
"std": 0.1538429439512892,
|
| 11 |
+
"n": 122
|
| 12 |
+
},
|
| 13 |
+
"ET": {
|
| 14 |
+
"mean": 0.6964991356739063,
|
| 15 |
+
"std": 0.1612273062938224,
|
| 16 |
+
"n": 122
|
| 17 |
+
},
|
| 18 |
+
"Mean": {
|
| 19 |
+
"mean": 0.7503796838217216
|
| 20 |
+
}
|
| 21 |
+
},
|
| 22 |
+
"config": {
|
| 23 |
+
"radius": 3,
|
| 24 |
+
"min_size": 50
|
| 25 |
+
}
|
| 26 |
+
}
|
gliomasam3_moe/vis_res/README.md
ADDED
|
@@ -0,0 +1,206 @@
|
|
|
|
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|
|
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|
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|
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|
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|
|
|
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|
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|
|
|
|
|
|
|
|
|
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|
|
|
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|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
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|
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|
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|
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|
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|
|
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|
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|
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|
|
|
|
|
| 1 |
+
# GliomaSAM3-MoE 可视化结果总结
|
| 2 |
+
|
| 3 |
+
本文档总结了各可视化实验的内容、目的和主要结论。
|
| 4 |
+
|
| 5 |
+
---
|
| 6 |
+
|
| 7 |
+
## 1. 主定性对比 (qualitative/)
|
| 8 |
+
|
| 9 |
+
**文件**: `Fig1_qualitative_comparison.png`
|
| 10 |
+
|
| 11 |
+
**内容**:
|
| 12 |
+
- 多模态输入(T1, T1ce, T2, FLAIR)
|
| 13 |
+
- Ground Truth 与预测结果对比
|
| 14 |
+
- 我们的方法 (GliomaSAM3-MoE) vs SegMamba
|
| 15 |
+
- WT/TC/ET 三区域分割叠加显示
|
| 16 |
+
|
| 17 |
+
**结论**: 展示模型在不同病例上的定性分割效果,通过彩色叠加可以直观比较各方法在肿瘤边界、区域完整性上的差异。
|
| 18 |
+
|
| 19 |
+
---
|
| 20 |
+
|
| 21 |
+
## 2. ET Gate 研究 (et_absent/)
|
| 22 |
+
|
| 23 |
+
**文件**: `Fig2_a_et_absent_BraTS-GLI-00012-000.png`
|
| 24 |
+
|
| 25 |
+
**内容**:
|
| 26 |
+
- ET Before Gate: 经过 gate 前的 ET 预测概率图
|
| 27 |
+
- ET After Gate: 经过 gate 后的 ET 预测概率图
|
| 28 |
+
- π_ET 值: 模型预测的 ET 存在概率
|
| 29 |
+
|
| 30 |
+
**结论**:
|
| 31 |
+
- π_ET 值反映模型对 ET(增强肿瘤)存在性的判断置信度
|
| 32 |
+
- 当 π_ET > 0.5 时,模型认为存在 ET;反之则抑制 ET 预测
|
| 33 |
+
- 此机制可帮助减少 ET 假阳性,但在当前训练下效果较弱(大多数 π_ET 接近 0.97-0.98)
|
| 34 |
+
|
| 35 |
+
---
|
| 36 |
+
|
| 37 |
+
## 3. 边界误差分析 (boundary/)
|
| 38 |
+
|
| 39 |
+
**文件**:
|
| 40 |
+
- `Fig3_a_boundary_BraTS-GLI-00005-000.png`
|
| 41 |
+
- `Fig3_b_boundary_BraTS-GLI-00017-000.png`
|
| 42 |
+
|
| 43 |
+
**内容**:
|
| 44 |
+
- 左侧: T1ce 图像 + Ground Truth 边界(白色)+ 预测边界(黑色)
|
| 45 |
+
- 右侧: 边界误差热力图(红色=假阳性FP,蓝色=假阴性FN)
|
| 46 |
+
|
| 47 |
+
**结论**:
|
| 48 |
+
- 边界误差热力图直观展示分割误差的空间分布
|
| 49 |
+
- 可用于分析 HD95 指标的改善区域
|
| 50 |
+
- 误差主要集中在肿瘤边缘模糊区域
|
| 51 |
+
|
| 52 |
+
---
|
| 53 |
+
|
| 54 |
+
## 4. 微小/碎片 ET 分析 (tiny_et/)
|
| 55 |
+
|
| 56 |
+
**文件**:
|
| 57 |
+
- `Fig4_a_tiny_et_BraTS-GLI-00005-000.png`
|
| 58 |
+
- `Fig4_b_tiny_et_BraTS-GLI-00006-000.png`
|
| 59 |
+
|
| 60 |
+
**内容**:
|
| 61 |
+
- 局部 ROI 放大显示
|
| 62 |
+
- Ground Truth vs 我们的方法 vs SegMamba
|
| 63 |
+
- 专注于 ET 极小或碎片化区域
|
| 64 |
+
|
| 65 |
+
**结论**: 展示模型对微小 ET 区域的捕获能力,验证是否能保留碎片化结构而不丢失或过度平滑。
|
| 66 |
+
|
| 67 |
+
---
|
| 68 |
+
|
| 69 |
+
## 5. MoE 路由可解释性 (moe_routing/)
|
| 70 |
+
|
| 71 |
+
**文件**:
|
| 72 |
+
- `Fig5_a_moe_routing_BraTS-GLI-00018-000.png`
|
| 73 |
+
- `Fig5_b_moe_routing_BraTS-GLI-00012-000.png`
|
| 74 |
+
|
| 75 |
+
**内容**:
|
| 76 |
+
- 柱状图展示各专家对 WT/TC/ET 三个区域的贡献权重
|
| 77 |
+
- X 轴: 专家索引 (E0-E4),激活的专家用 "(active)" 标注
|
| 78 |
+
- Y 轴: 贡献值
|
| 79 |
+
- 颜色区分: WT(青色), TC(品红), ET(黄色)
|
| 80 |
+
- 黑色折线: 路由权重 γ,激活专家标注具体值
|
| 81 |
+
- 非激活专家显示为半透明(alpha=0.3)
|
| 82 |
+
|
| 83 |
+
**重要说明**:
|
| 84 |
+
- 模型配置 `moe_topk: 2`,即采用 **Top-2 稀疏门控**
|
| 85 |
+
- 每次推理**只激活 2 个专家**,其余专家权重为 0
|
| 86 |
+
- 这是 Mixture-of-Experts 的标准设计,不是 bug
|
| 87 |
+
|
| 88 |
+
**结论**:
|
| 89 |
+
- Top-2 稀疏门控使计算效率提高,同时保持模型容量
|
| 90 |
+
- 不同案例可能激活不同的专家组合(如 E0+E2 或其他)
|
| 91 |
+
- 路由权重 γ 显示各激活专家的相对重要性
|
| 92 |
+
|
| 93 |
+
---
|
| 94 |
+
|
| 95 |
+
## 6. 概念 Token 可解释性 (concept_tokens/)
|
| 96 |
+
|
| 97 |
+
每个病例生成 3 张图:
|
| 98 |
+
|
| 99 |
+
### 6.1 ET 预测概览 (Fig6_X1_et_overview_*.png)
|
| 100 |
+
- 左: T1ce 原始输入
|
| 101 |
+
- 右: ET 预测 mask 叠加 + 体素总数
|
| 102 |
+
|
| 103 |
+
### 6.2 碎片化分析 (Fig6_X2_fragmentation_*.png)
|
| 104 |
+
- 左: 连通域可视化(不同颜色标识各组件)
|
| 105 |
+
- 中: 各组件大小柱状图
|
| 106 |
+
- 右: FRAG_BIN 分类(None/Low/Medium/High)
|
| 107 |
+
|
| 108 |
+
### 6.3 规模分析 (Fig6_X3_scale_*.png)
|
| 109 |
+
- 左: ET 区域可视化
|
| 110 |
+
- 右: SCALE_BIN 分类(Tiny/Small/Medium/Large)
|
| 111 |
+
|
| 112 |
+
**结论**:
|
| 113 |
+
- **FRAG_BIN**: 根据 ET 连通域数量判断碎片化程度
|
| 114 |
+
- n ≤ 1 → None, n ≤ 3 → Low, n ≤ 5 → Medium, n > 5 → High
|
| 115 |
+
- **SCALE_BIN**: 根据 ET 体素总数判断规模
|
| 116 |
+
- voxels ≤ 50 → Tiny, ≤ 200 → Small, ≤ 500 → Medium, > 500 → Large
|
| 117 |
+
- 这些概念 token 与肿瘤形态特征直接关联,可用于辅助临床决策
|
| 118 |
+
|
| 119 |
+
---
|
| 120 |
+
|
| 121 |
+
## 7. 双域增强效果 (dual_domain/)
|
| 122 |
+
|
| 123 |
+
**文件**:
|
| 124 |
+
- `Fig7_a_dual_domain_BraTS-GLI-00005-000.png`
|
| 125 |
+
- `Fig7_b_dual_domain_BraTS-GLI-00017-000.png`
|
| 126 |
+
|
| 127 |
+
**内容**:
|
| 128 |
+
- 左: 原始图像的傅里叶幅度谱
|
| 129 |
+
- 右: 增强后的傅里叶幅度谱
|
| 130 |
+
- 统一色标便于比较
|
| 131 |
+
|
| 132 |
+
**结论**:
|
| 133 |
+
- 频域可视化展示模型如何利用频谱信息
|
| 134 |
+
- 增强后的幅度谱可能显示高频成分增强,有助于边界检测
|
| 135 |
+
- 体现双域(空域+频域)融合的效果
|
| 136 |
+
|
| 137 |
+
---
|
| 138 |
+
|
| 139 |
+
## 8. AmpMix 增强鲁棒性 (ampmix/)
|
| 140 |
+
|
| 141 |
+
**文件**: `Fig8_a_ampmix_BraTS-GLI-00005-000.png`
|
| 142 |
+
|
| 143 |
+
**内容**:
|
| 144 |
+
- 左: 原始图像 + 预测
|
| 145 |
+
- 中: AmpMix 扰动后的图像
|
| 146 |
+
- 右: 扰动后的预测结果
|
| 147 |
+
|
| 148 |
+
**结论**:
|
| 149 |
+
- AmpMix 通过混合不同样本的傅里叶幅度谱进行数据增强
|
| 150 |
+
- 展示模型在幅度谱扰动下的预测稳定性
|
| 151 |
+
- 理想情况下,扰动前后预测应保持一致,边界不发生显著漂移
|
| 152 |
+
|
| 153 |
+
---
|
| 154 |
+
|
| 155 |
+
## 9. 失败案例分析 (failure/)
|
| 156 |
+
|
| 157 |
+
**文件**: `Fig9_a_failure_BraTS-GLI-00020-000.png`
|
| 158 |
+
|
| 159 |
+
**内容**:
|
| 160 |
+
- 左: Ground Truth
|
| 161 |
+
- 右: 预测结果
|
| 162 |
+
- 标注: 失败原因说明
|
| 163 |
+
|
| 164 |
+
**结论**:
|
| 165 |
+
- 展示模型的局限性
|
| 166 |
+
- 典型失败原因包括:
|
| 167 |
+
- 边界模��区域的判断困难
|
| 168 |
+
- 低对比度区域的误分割
|
| 169 |
+
- 伪影或异常强度影响
|
| 170 |
+
- 诚实展示模型限制有助于后续改进方向
|
| 171 |
+
|
| 172 |
+
---
|
| 173 |
+
|
| 174 |
+
## 文件结构
|
| 175 |
+
|
| 176 |
+
```
|
| 177 |
+
vis_res/
|
| 178 |
+
├── README.md # 本文档
|
| 179 |
+
├── qualitative/ # 主定性对比
|
| 180 |
+
├── et_absent/ # ET Gate 研究
|
| 181 |
+
├── boundary/ # 边界误差分析
|
| 182 |
+
├── tiny_et/ # 微小 ET 分析
|
| 183 |
+
├── moe_routing/ # MoE 路由可解释性
|
| 184 |
+
├── concept_tokens/ # 概念 Token 可解释性
|
| 185 |
+
├── dual_domain/ # 双域增强效果
|
| 186 |
+
├── ampmix/ # AmpMix 鲁棒性
|
| 187 |
+
├── failure/ # 失败案例
|
| 188 |
+
└── aux_cache/ # 中间结果缓存(内部使用)
|
| 189 |
+
```
|
| 190 |
+
|
| 191 |
+
---
|
| 192 |
+
|
| 193 |
+
## 生成方式
|
| 194 |
+
|
| 195 |
+
所有可视化由 `visualizations/vis_publication.py` 生成,配置文件为 `visualizations/vis_config.yaml`。
|
| 196 |
+
|
| 197 |
+
```bash
|
| 198 |
+
cd /root/githubs/gliomasam3_moe
|
| 199 |
+
PYTHONPATH=/root/githubs/sam3:$PYTHONPATH python visualizations/vis_publication.py \
|
| 200 |
+
--config visualizations/vis_config.yaml \
|
| 201 |
+
--model-config configs/train.yaml \
|
| 202 |
+
--checkpoint ./logs/segmamba/model/ckpt_step600.pt \
|
| 203 |
+
--run all
|
| 204 |
+
```
|
| 205 |
+
|
| 206 |
+
可通过 `--run <name>` 单独生成特定可视化(如 `--run moe,dual_domain`)。
|
gliomasam3_moe/vis_res/ampmix/Fig8_a_ampmix_BraTS-GLI-00005-000.pdf
ADDED
|
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