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@@ -22,6 +22,8 @@ Checkpoints behind the [CELL-FM CondenSeq demo](https://huggingface.co/spaces/Bo
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  | `hpa/vae.bin` | Image VAE at 256x256, the one `hpa/cellfm_seq2img.bin` was trained against | `pretrain_hpa/vae/checkpoint-50000` |
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  | `hpa/cellfm_img2seq.bin` | CELL-FM image-to-sequence model for HPA, 512x512, 3-channel conditioning (includes the ESM-C 600M encoder) | `pretrain_hpa/cellfm_img2seq/checkpoint-60000` |
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  | `hpa/vae_512.bin` | Image VAE at 512x512, the one `hpa/cellfm_img2seq.bin` was trained against — a different model from `hpa/vae.bin`, not a rename | `pretrain_hpa/vae_512/checkpoint-50000` |
 
 
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  | `hpa/anchor_cell.npy` | The fixed cell every NLS-screening image is conditioned on: `(3, 256, 256)` float32 in [-1, 1], channels nucleus, ER, microtubules. HPA gene H3C13, cell crop `1194_B2_2_4` | built |
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  | `hpa/anchor_masks.npz` | Two 256x256 boolean masks over that cell, `nucleus` and `cell`; cytoplasm is `cell & ~nucleus` | built |
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  | `hpa/pls_anchor_nls.npz` | The cell PLS generation conditions on for nuclear signals: `cell` `(3, 512, 512)` nucleus/ER/microtubules and `protein` `(1, 512, 512)`, float32 in [-1, 1]. HPA gene PPM1G (Nucleoplasm), crop `392_B9_1_11` | built |
@@ -36,7 +38,9 @@ Hyperparameters for the CondenSeq models are set in `pipeline.py` in the Space a
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  hyperparameters are spelled out in `notebooks/nls_screening.ipynb` and mirror
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  `scripts/cell_fm/evaluate_virtual_staining_hpa_dict.sh`. The img2seq pair mirrors
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  `scripts_local/cell_fm/evaluate_img2seq_hpa_v2.sh`: 512 px, `sample_size` 128,
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- `encoder_patch_size` 8, `img_generator_patch_size` 4, 8 attention heads.
 
 
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  Each generator must be loaded with the VAE it was trained against — pairing
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  `cellfm_img2seq.bin` with the 256 px `vae.bin` gives a latent-size mismatch.
 
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  | `hpa/vae.bin` | Image VAE at 256x256, the one `hpa/cellfm_seq2img.bin` was trained against | `pretrain_hpa/vae/checkpoint-50000` |
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  | `hpa/cellfm_img2seq.bin` | CELL-FM image-to-sequence model for HPA, 512x512, 3-channel conditioning (includes the ESM-C 600M encoder) | `pretrain_hpa/cellfm_img2seq/checkpoint-60000` |
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  | `hpa/vae_512.bin` | Image VAE at 512x512, the one `hpa/cellfm_img2seq.bin` was trained against — a different model from `hpa/vae.bin`, not a rename | `pretrain_hpa/vae_512/checkpoint-50000` |
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+ | `opencell/cellfm_seq2img.bin` | CELL-FM virtual-staining generator for OpenCell, 256x256, single nucleus conditioning channel, fine-tuned (includes the ESM-C 600M encoder) | `finetune_opencell/cellfm_vs/checkpoint-100000` |
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+ | `opencell/vae.bin` | Image VAE at 256x256, the one `opencell/cellfm_seq2img.bin` was trained against — OpenCell-finetuned, so not interchangeable with `hpa/vae.bin` despite the matching shape | `finetune_opencell/vae/checkpoint-50000` |
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  | `hpa/anchor_cell.npy` | The fixed cell every NLS-screening image is conditioned on: `(3, 256, 256)` float32 in [-1, 1], channels nucleus, ER, microtubules. HPA gene H3C13, cell crop `1194_B2_2_4` | built |
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  | `hpa/anchor_masks.npz` | Two 256x256 boolean masks over that cell, `nucleus` and `cell`; cytoplasm is `cell & ~nucleus` | built |
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  | `hpa/pls_anchor_nls.npz` | The cell PLS generation conditions on for nuclear signals: `cell` `(3, 512, 512)` nucleus/ER/microtubules and `protein` `(1, 512, 512)`, float32 in [-1, 1]. HPA gene PPM1G (Nucleoplasm), crop `392_B9_1_11` | built |
 
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  hyperparameters are spelled out in `notebooks/nls_screening.ipynb` and mirror
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  `scripts/cell_fm/evaluate_virtual_staining_hpa_dict.sh`. The img2seq pair mirrors
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  `scripts_local/cell_fm/evaluate_img2seq_hpa_v2.sh`: 512 px, `sample_size` 128,
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+ `encoder_patch_size` 8, `img_generator_patch_size` 4, 8 attention heads. The OpenCell pair
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+ mirrors `scripts/cell_fm/evaluate_virtual_staining_opencell.sh`: 256 px, `sample_size` 64,
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+ `encoder_patch_size` 4, `img_generator_patch_size` 2, 18 attention heads, `cell_image` `nucl`.
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  Each generator must be loaded with the VAE it was trained against — pairing
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  `cellfm_img2seq.bin` with the 256 px `vae.bin` gives a latent-size mismatch.