Large-scale Pretraining for Molecular Property Prediction
This repository is an official implementation of a model which won first place in the Samsung AI Challenge for Scientific Discovery competition and was introduced at SAIF 2021. The result of the challenge was announced at this video.
MoT is a transformer-based model for predicting molecular properties from its 3D molecular structure. It was first introduced to calculate the excitation energy gap between S1 and T1 states by the molecular structure.
Before running this project, you need to install the below libraries:
- numpy
- pandas
- torch==1.9.0+cu111
- tqdm
- wandb
- dataclasses
- requests
- omegaconf
- pytorch_lightning==1.4.8
- rdkit-pypi
- scikit_learn
This project supports NVIDIA Apex. It will be automatically detected and used to accelerate training when installed. apex reduces the training time up to 50%.
setup.sh helps installing necessary libraries, including apex. It installs the requirements and apex at once. You can simply run the script as follows:
$ bash setup.shThere are many apporaches to predict the molecular properties. However, for the case of calculating excitation energy gaps (e.g. between S1 to T1 states), it is necessary to consider the entire 3D structure and the charge of atoms in the compound. But many transformer-based molecular models use SMILES (or InChI) format. We also tried text-based methods in the competition, but the graph-based models showed better performance.
The important thing is to consider all connections between the atoms in the compound. However, the atoms are placed in 3D coordinate system, and it is almost impossible to feed 3D positional informations to the model (and adding 3d positional embeddings was worse than the baseline). So we designed new attention method, inspired by disentangled attention in DeBERTa.
First of all, the type of atoms and their charges will be embedded to the vectors and summed. Note that the positional embeddings will not be used to the input because attention layers will calculate the attention scores relatively. And thanks to the absence of the positional embeddings, there is no limit to the number of atoms.
The hidden representations will be attended by the attention layers. Similar to the disentangled attention introduced in DeBERTa, our relative attention is performed not only for contents, but also between relative informations and the contents. The relative informations include relative distances and the type of bonds between the atoms.
The relative information R is calculated as above. The euclidean distances are encoded through sinusoidal encoding, with modified period (from 10000 to 100). The bond type embeddings can be described as below:
The important thing is disconnections (i.e. there is no bond between two certain atoms) should be embedded as index 0, rather than excluded from attention. Also [CLS] tokens are separated from other normal bond-type embeddings on relative attention.
According to the above architecture, the model successfully focuses on the relations of the atoms. And similar to the other transformer-based models, it also shows that pretraining from large-scale dataset achieves better performance, even with few finetuning samples. We pretrained our model with PubChem3D (50M) and PubChemQC (3M). For PubChem3D, the model was trained to predict conformer-RMSD, MMFF94 energy, shape self-overlap, and feature self-overlap. For PubChemQC, the model was trained to predict the singlet excitation energies from S1 to S10 states.
To reproduce our results on the competition or pretrain a new model, you should follow the below steps. A large disk and high-performance GPUs (e.g. A100s) will be required.
First of all, let's download PubChem3D and PubChemQC datasets. The following commands will download the datasets and format to the specific dataset structure.
$ python utilities/download_pubchem.py
$ python utilities/download_pubchemqc.pyAlthough we used 50M PubChem3D compounds, you can use full 100M samples if your network status and the client are available while downloading.
After downloading all datasets, we have to create index files which indicate the seeking position of each sample. Because the dataset size is really large, it is impossible to load the entire data to the memory. So our dataset will access the data randomly using this index files.
$ python utilities/create_dataset_index.py pubchem-compound-50m.csv
$ python utilities/create_dataset_index.py pubchemqc-excitations-3m.csvCheck if pubchem-compound-50m.index and pubchemqc-excitations-3m.index are created.
Now we are ready to train MoT. Using the datasets, we are going to pretrain new model. Move the datasets to pretrain directory and also change the working directory to pretrain. And type the below commands to pretrain for PubChem3D and PubChemQC datasets respectively. Note that PubChemQC-pretraining will use PubChem3D-pretrained model weights.
$ python src/train.py config/mot-base-pubchem.yaml
$ python src/train.py config/mot-base-pubchemqc.yamlCheck if mot-base-pubchem.pth and mot-base-pubchemqc.pth are created. Next, move the final output weights file (mot-base-pubchemqc.pth) to finetune directory. Prepare the competition dataset samsung-ai-challenge-for-scientific-discovery to the same directory and start finetuning by using below command:
$ python src/train.py config/train/mot-base-pubchemqc.yaml \
data.fold_index=[fold index] \
model.random_seed=[random seed]We recommend to train the model for 5 folds with various random seeds. It is well known that the random seed is critial to transformer finetuning. You can tune the random seed to achieve better results.
After finetuning the models, use following codes to predict the energy gaps through test dataset.
$ python src/predict.py config/predict/mot-base-pubchemqc.yaml \
model.pretrained_model_path=[finetuned model path]And you can see the prediction file of which name is same as the model name. You can submit the single predictions or average them to get ensembled result.
$ python utilities/simple_ensemble.py finetune/*.csv [output file name]If you want to finetune with custom dataset, all you need to do is to rewrite the configuration file. Note that finetune directory is considered only for the competition dataset. So the entire training codes are focused on the competition data structure. Instead, you can finetune the model with your custom dataset on pretrain directory. Let's check the configuration file for PubChemQC dataset which is placed at pretrain/config/mot-base-pubchemqc.yaml.
data:
dataset_file:
label: pubchemqc-excitations-3m.csv
index: pubchemqc-excitations-3m.index
input_column: structure
label_columns: [s1_energy, s2_energy, s3_energy, s4_energy, s5_energy, s6_energy, s7_energy, s8_energy, s9_energy, s10_energy]
labels_mean_std:
s1_energy: [4.56093558, 0.8947327]
s2_energy: [4.94014921, 0.8289951]
s3_energy: [5.19785427, 0.78805644]
s4_energy: [5.39875606, 0.75659831]
s5_energy: [5.5709758, 0.73529373]
s6_energy: [5.71340364, 0.71889017]
s7_energy: [5.83764871, 0.70644563]
s8_energy: [5.94665475, 0.6976438]
s9_energy: [6.04571037, 0.69118142]
s10_energy: [6.13691953, 0.68664366]
max_length: 128
bond_drop_prob: 0.1
validation_ratio: 0.05
dataloader_workers: -1
model:
pretrained_model_path: mot-base-pubchem.pth
config: ...In the configuration file, you can see data.dataset_file field. It can be changed to the desired finetuning dataset with its index file. Do not forget to create the index file by utilities/create_dataset_index.py. And you can specify the column name which contains the encoded 3D structures. data.label_columns indicates which columns will be used to predict. The values will be normalized by data.labels_mean_std. Simply copy this file and rename to your own dataset. Change the name and statistics of each label. Here is an example for predicting toxicity values:
data:
dataset_file:
label: toxicity.csv
index: toxicity.index
input_column: structure
label_columns: [toxicity]
labels_mean_std:
toxicity: [0.92, 1.85]
max_length: 128
bond_drop_prob: 0.0
validation_ratio: 0.1
dataloader_workers: -1
model:
pretrained_model_path: mot-base-pubchemqc.pth
config:
num_layers: 12
hidden_dim: 768
intermediate_dim: 3072
num_attention_heads: 12
hidden_dropout_prob: 0.1
attention_dropout_prob: 0.1
position_scale: 100.0
initialize_range: 0.02
train:
name: mot-base-toxicity
optimizer:
lr: 1e-4
betas: [0.9, 0.999]
eps: 1e-6
weight_decay: 0.01
training_steps: 100000
warmup_steps: 10000
batch_size: 256
accumulate_grads: 1
max_grad_norm: 1.0
validation_interval: 1.0
precision: 16
gpus: 1| Model | PubChem | PubChemQC | Competition LB (Public/Private) |
|---|---|---|---|
| ELECTRA | 0.0493 | − | 0.1508/− |
| BERT Regression | 0.0074 | 0.0497 | 0.1227/− |
| MoT-Base (w/o PubChem) | − | 0.0188 | 0.0877/− |
| MoT-Base (PubChemQC 150k) | 0.0086 | 0.0151 | 0.0666/− |
|     + PubChemQC 300k | " | 0.0917 | 0.0526/− |
|     + 5Fold CV | " | " | 0.0507/− |
|     + Ensemble | " | " | 0.0503/− |
| Â Â Â Â + Increase Maximum Atoms | " | " | 0.0497/0.04931 |
Description: Comparison results of various models. ELECTRA and BERT Regression are SMILES-based models which are trained with PubChem-100M (and PubChemQC-3M for BERT Regression only). ELECTRA is trained to distinguish fake SMILES tokens (i.e., ELECTRA approach) and BERT Regression is trained to predict the labels, without unsupervised learning. PubChemQC 150k and 300k denote that the model is trained for 150k and 300k steps in PubChemQC stage.
This repository provides some useful utility scripts.
create_dataset_index.py: As mentioned above, it creates seeking positions of samples in the dataset for random accessing.download_pubchem.pyanddownload_pubchemqc.py: Download PubChem3D and PubChemQC datasets.find_test_compound_cids.py: Find CIDs of the compounds in test dataset to prevent from training the compounds. It may occur data-leakage.simple_ensemble.py: It performs simple ensemble by averaging all predictions from various models.
This repository is released under the Apache License 2.0. License can be found in LICENSE file.