Upload CREMI dataset (ssTEM neuron segmentation)
Browse files- .gitattributes +3 -0
- README.md +79 -0
- train/sample_A.hdf +3 -0
- train/sample_B.hdf +3 -0
- train/sample_C.hdf +3 -0
.gitattributes
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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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# 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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train/sample_A.hdf filter=lfs diff=lfs merge=lfs -text
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train/sample_B.hdf filter=lfs diff=lfs merge=lfs -text
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train/sample_C.hdf filter=lfs diff=lfs merge=lfs -text
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README.md
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# CREMI - Circuit Reconstruction from Electron Microscopy Images
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## Dataset Description
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CREMI is a benchmark dataset for evaluating algorithms for automatic reconstruction of neurons and neuronal connectivity from serial section electron microscopy data.
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### Modality
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- Serial section Transmission Electron Microscopy (ssTEM)
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### Anatomy
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- Adult Drosophila melanogaster brain
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### Segmentation Targets
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- **Neuron segmentation** (`volumes/labels/neuron_ids`)
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- **Synaptic cleft segmentation** (`volumes/labels/clefts`)
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### Volume Size
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- 125 slices × 1250 × 1250 pixels per sample
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- Resolution: 4×4×40 nm (x,y,z)
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## Dataset Structure
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```
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CREMI/
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└── train/
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├── sample_A.hdf # 167 MB
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├── sample_B.hdf # 160 MB
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└── sample_C.hdf # 165 MB
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```
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Note: Test files (A+, B+, C+) are not included as they have no labels.
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## HDF5 Structure
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Each training file contains:
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- `volumes/raw`: (125, 1250, 1250) uint8 - grayscale EM images
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- `volumes/labels/neuron_ids`: (125, 1250, 1250) uint64 - neuron instance segmentation
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- `volumes/labels/clefts`: (125, 1250, 1250) uint64 - synaptic cleft segmentation
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- `annotations/` - synaptic partner annotations
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## Usage
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```python
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import h5py
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from huggingface_hub import hf_hub_download
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# Download a training volume
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path = hf_hub_download(
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repo_id="Angelou0516/CREMI",
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filename="train/sample_A.hdf",
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repo_type="dataset"
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)
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# Load data
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with h5py.File(path, 'r') as f:
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raw = f['volumes/raw'][:] # (125, 1250, 1250)
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neuron_ids = f['volumes/labels/neuron_ids'][:] # (125, 1250, 1250)
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clefts = f['volumes/labels/clefts'][:] # (125, 1250, 1250)
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```
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## Citation
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```bibtex
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@misc{cremi2016,
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title={CREMI: MICCAI Challenge on Circuit Reconstruction from Electron Microscopy Images},
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author={Funke, Jan and Saalfeld, Stephan and Bock, Davi and Turaga, Srini and Perlman, Eric},
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year={2016},
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url={https://cremi.org/}
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}
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```
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## License
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Please refer to the original dataset website: https://cremi.org/
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## Links
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- [CREMI Challenge Website](https://cremi.org/)
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- [CREMI Data Page](https://cremi.org/data/)
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- [CREMI Metrics](https://cremi.org/metrics/)
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train/sample_A.hdf
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version https://git-lfs.github.com/spec/v1
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oid sha256:4c563d1b78acb2bcfb3ea958b6fe1533422f7f4a19f3e05b600bfa11430b510d
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size 175159177
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train/sample_B.hdf
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version https://git-lfs.github.com/spec/v1
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oid sha256:887e85521e00deead18c94a21ad71f278d88a5214c7edeed943130a1f4bb48b8
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size 167293425
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train/sample_C.hdf
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version https://git-lfs.github.com/spec/v1
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oid sha256:2874496f224d222ebc29d0e4753e8c458093e1d37bc53acd1b69b19ed1ae7052
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size 173102370
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