This repository is the official implementation of KANO, which is model proposed in a paper: Knowledge graph-enhanced molecular contrastive learning with functional prompt.
2024-2We've released ChatCell, a new paradigm that leverages natural language to make single-cell analysis more accessible and intuitive. Please visit our homepage and Github page for more information.2024-1Our paper Domain-Agnostic Molecular Generation with Chemical Feedback is accepted by ICLR 2024.2024-1Our paper Mol-Instructions: A Large-Scale Biomolecular Instruction Dataset for Large Language Models is accepted by ICLR 2024.2023-6We release Mol-Instructions, a large-scale biomolecule instruction dataset for large language models.2023-3We propose MolGen, a robust pre-trained molecular generative model with self-feedback.
We propose a Knowledge graph-enhanced molecular contrAstive learning with fuNctional prOmpt (KANO), exploiting fundamental domain knowledge in both pre-training and fine-tuning.
Firstly, we construct a Chemical Element Knowledge Graph (ElementKG) based on the Periodic Table and Wikipedia pages to summarize the class hierarchy, relations and chemical attributes of elements and functional groups.
Second, we propose an element-guided graph augmentation in contrastive-based pre-training to capture deeper associations inside molecular graphs.
Third, to bridge the gap between the pre-training contrastive tasks and downstream molecular property prediction tasks, we propose functional prompts to evoke the downstream task-related knowledge acquired by the pre-trained model.
To run our code, please install dependency packages.
python 3.7
torch 1.13.1
rdkit 2018.09.3
numpy 1.20.3
gensim 4.2.0
nltk 3.4.5
owl2vec-star 0.2.1
Owlready2 0.37
torch-scatter 2.0.9
This project mainly contains the following parts.
├── chemprop # molecular graph preprocessing, data splitting, loss function and graph encoder
├── data # sore the molecular datasets for pre-training and fine-tuning
│ ├── bace.csv # downstream dataset BACE
│ ├── bbbp.csv # downstream dataset BBBP
│ ├── clintox.csv # downstream dataset ClinTox
│ ├── esol.csv # downstream dataset ESOL
│ ├── freesolv.csv # downstream dataset FreeSolv
│ ├── hiv.csv # downstream dataset HIV
│ ├── lipo.csv # downstream dataset Lipophilicity
│ ├── muv.csv # downstream dataset MUV
│ ├── qm7.csv # downstream dataset QM7
│ ├── qm8.csv # downstream dataset QM8
│ ├── qm9.csv # downstream dataset QM9
│ ├── sider.csv # downstream dataset SIDER
│ ├── tox21.csv # downstream dataset Tox21
│ ├── toxcast.csv # downstream dataset ToxCast
│ └── zinc15_250K.csv # pre-train dataset ZINC250K
├── dumped # store the training log and checkpoints of the model
│ └── pretrained_graph_encoder # the pre-trained model
├── finetune.sh # conduct fine-tuning
├── initial # store the embeddings of ElementKG, and preprocess it for the model
├── KGembedding # store ElementKG, and get the embeddings of eneities and relations in ElementKG
├── pretrain.py # conduct pre-training
└── train.py # training code for fine-tuning
If you want to use our pre-trained model directly for molecular property prediction, please run the following command:
>> bash finetune.sh| Parameter | Description | Default Value |
|---|---|---|
| data_path | Path to downstream tasks data files (.csv) | None |
| metric | Metric to use during evaluation. | Defaults to "auc" for classification and "rmse" for regression. |
| dataset_type | Type of dataset, e.g. classification or regression, this determines the loss function used during training. | 'regression' |
| epochs | Number of epochs to run | 30 |
| num_folds | Number of folds when performing cross validation | 1 |
| gpu | Which GPU to use | None |
| batch_size | Batch size | 50 |
| seed | Random seed to use when splitting data into train/val/test sets. When num_folds > 1, the first fold uses this seed and all subsequent folds add 1 to the seed. |
1 |
| init_lr | Initial learning rate | 1e-4 |
| split_type | Method of splitting the data into train/val/test (random/ scaffold splitting/ cluster splitting) | 'random' |
| step | Training phases (pre-training, fine-tuning with functional prompts or with other architectures) | 'functional_prompt' |
| exp_name | Experiment name | None |
| exp_id | Experiment ID | None |
| checkpoint_path | Path to pre-trained model checkpoint (.pt file) | None |
Note that if you change the data_path, don't forget to change the corresponding metric, dataset_type and split_type! For example:
>> python train.py \
--data_path ./data/qm7.csv \
--metric 'mae' \
--dataset_type regression \
--epochs 100 \
--num_runs 20 \
--gpu 1 \
--batch_size 256 \
--seed 43 \
--init_lr 1e-4 \
--split_type 'scaffold_balanced' \
--step 'functional_prompt' \
--exp_name finetune \
--exp_id qm7 \
--checkpoint_path "./dumped/pretrained_graph_encoder/original_CMPN_0623_1350_14000th_epoch.pkl"ElementKG is stored in KGembedding/elementkg.owl. If you want to train the model yourself to obtain the embeddings of eneities and relations in ElementKG, please run $ python run.py. This may take a few minutes to complete. For your convenience, we provide the trained representaions, stored in initial/elementkgontology.embeddings.txt
After obtaining the embeddings of ElementKG, we need to preprocess it in order to utilize it in pre-training. Please excute cd KANO/initial and run $ python get_dict.py to get the processed file. Of course, we also provide processed files in initial, so that you can directly proceed to the next step.
We collect 250K unlabeled molecules sampled from the ZINC 15 datasets to pre-train KANO. The pre-training data can be found in data/zinc15_250K.csv. If you want to pre-train the model with the pre-training data, please run:
>> python pretrain.py --exp_name 'pre-train' --exp_id 1 --step pretrain| Parameter | Description | Default Value |
|---|---|---|
| data_path | Path to pre-training data files (.csv) | None |
| epochs | Number of epochs to run | 30 |
| gpu | Which GPU to use | None |
| batch_size | Batch size | 50 |
You can change these parameters directly in pretrain.py. In our setting, we set epochs and batch_size to 50 and 1024, respectively. We also provided pre-trained models, which you can download from dumped/pretrained_graph_encoder/original_CMPN_0623_1350_14000th_epoch.pkl.
The operational details of this part are the same as the section Quick start.
We also provide other options in this code repository.
Our code supports using cluster splitting to split downstream datasets, as detailed in the paper. You can set thesplit_type parameter to cluster_balanced to perform cluster splitting.
Besides functional prompts, we also support testing other ways of incorporating functional group knowledge. By setting the step parameter to finetune_add or finetune_concat, you achieve adding or concatenating functional group knowledge with the original molecular representation, respectively.
We also support specifying a dataset as the input for the train/val/test sets by setting the parameters data_path, separate_test_path and separate_val_path to the location of the specified train/val/test data.
We now support making predictions with fine-tuned models. Use the command python predict.py --exp_name pred --exp_id pred. Remember to specify the checkpoint_path (with a .pt suffix) and the path for the prediction data (with the header as 'smiles').
Thanks for the following released code bases:
Should you have any questions, please feel free to contact Miss Yin Fang at [email protected].
If you use or extend our work, please cite the paper as follows:
@article{fang2023knowledge,
title={Knowledge graph-enhanced molecular contrastive learning with functional prompt},
author={Fang, Yin and Zhang, Qiang and Zhang, Ningyu and Chen, Zhuo and Zhuang, Xiang and Shao, Xin and Fan, Xiaohui and Chen, Huajun},
journal={Nature Machine Intelligence},
pages={1--12},
year={2023},
publisher={Nature Publishing Group UK London}
}
