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COMO

PyTorch
chemistry
cheminformatics
optical-chemical-structure-recognition
ocsr
molecule-recognition
smiles
transformer
swin-transformer
minimum-risk-training
molecular-graph
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@@ -142,8 +142,7 @@ Please refer to the original sources for attribution:
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  | Dataset | Source |
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  |---------|--------|
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  | USPTO, CLEF, JPO, UOB, Staker | [Rajan et al., 2020](https://github.com/Kohulan/DECIMER-Image_Transformer), [Xiong et al., 2023](https://github.com/jiachengxiong/alpha-Extractor) |
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- | Staker | []() |
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- | Indigo, ChemDraw, ACS | [Qian et al., 2023](https://github.com/thomas0809/MolScribe) |
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  | USPTO-10K | [Morin et al., 2023](https://github.com/DS4SD/molgrapher) |
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  | WildMol-10K | [Fang et al., 2025](https://github.com/orgs/Chem-Struct-ML/repositories) |
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  | Dataset | Source |
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  |---------|--------|
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  | USPTO, CLEF, JPO, UOB, Staker | [Rajan et al., 2020](https://github.com/Kohulan/DECIMER-Image_Transformer), [Xiong et al., 2023](https://github.com/jiachengxiong/alpha-Extractor) |
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+ | Indigo, ChemDraw, ACS, Staker | [Qian et al., 2023](https://github.com/thomas0809/MolScribe) |
 
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  | USPTO-10K | [Morin et al., 2023](https://github.com/DS4SD/molgrapher) |
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  | WildMol-10K | [Fang et al., 2025](https://github.com/orgs/Chem-Struct-ML/repositories) |
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