GeminiMol

Refer to GitHub.

<h1 align="left"> GeminiMol </h1> <h3 align="left"> Molecular Representation Model Enhanced by Conformational Space Profile </h3> <p align="left"> 📃 <a href="https://www.biorxiv.org/content/10.1101/2023.12.14.571629" target="_blank">Paper</a> · 🤗 <a href="https://huggingface.co/AlphaMWang/GeminiMol" target="_blank">Model</a> · 📕 <a href="https://zenodo.org/records/10450788" target="_blank">Data</a><br> </p> <p align="right"> <img style="float: right" src="imgs/geminimol.png" alt="alt text" width="550px" align="right"/> </p>

This repository provides the official implementation of the GeminiMol model, training data, and utilities. In this work, we propose a hybrid contrastive learning framework, which conducts inter-molecular contrastive learning by multiple projection heads of conformational space similarities (CSS). Please also refer to our paper for a detailed description of GeminiMol.

Table of Contents

• Table of Contents
• 💗 Motivation
• 💡 Highlight
• 🔔 News
• 😫 Limitations
• 📕 Installation
  • Download datasets and models
  • Installing the dependency packages
• 📓 Application
  • Virtual Screening and Target Identification
  • Molecular Proptery Modeling (QSAR and ADMET)
  • Molecular Clustering
  • Extract Molecular Features (GeminiMol Encoding)
• 👐 Reproducing
  • Download Training and Benchmark Datasets
  • Re-training our models
  • Benchmarking the fingerprints and our models
• ⭐ Citing This Work
• ✅ License
• 💌 Get in Touch
• 😃 Acknowledgements

💗 Motivation

The molecular representation model is an emerging artificial intelligence technology for extracting features of small molecules. Inspired by the dynamics of small molecules in solution, introducing the conformational space profile into molecular representation models is a promising aim. The conformational space profile covers the heterogeneity of molecule properties, such as the multi-target mechanism of drug action, recognition of different biomolecules, dynamics in cytoplasm and membrane, which may facilitate further downstream application and generalization capability of molecular representation model.

💡 Highlight

• GeminiMol exhibits the capability to identify molecular pairs with similar 3D active conformers, even in scenarios where their 2D structures exhibit significant differences.
• GeminiMol was pre-trained on only 37,336 molecular structures, yet it can generalize to zero-shot and QSAR tasks involving millions of molecules.
• GeminiMol shown the balanced performance across various applications, including virtual screening, target identification, and cellular phenotype-based property modeling.

🔔 News

• 2023-12, our paper has been uploaded to BioRxiv, you can find it here.
• 2024-01, we have released PharmProfiler.py, which facilitates virtual screening and target identification.
• 2024-03, we have released PropPredictor.py, which facilitates the deployment and repurposing of QSAR and ADMET prediction models.

😫 Limitations

• Note that, the conformational space profile is not a panacea for drug discovery. For a portion of tasks, the 2D structure of a compound already contains sufficient information to establish structure-activity relationships, rendering the introduction of the conformational space profile inconsequential for these tasks.
• The evaluation of intermolecular similarity is not limited to pharmacophore similarity in 3D conformational space and maximum common substructure similarity in 2D structures. By incorporating additional intermolecular similarity metrics during pre-training, we can further enrich the knowledge that the model can learn, such as molecular fingerprints and molecular surface potentials.
• Due to computational resource limitations, we only included 39,290 molecules in our pre-training. It is foreseeable that incorporating more molecular structures during pre-training could further enhance the performance of GeminiMol, particularly when guided by drug-target relationships to obtain high-quality data.

📕 Installation

GeminiMol is a pytorch-based AI model. To set up the GeminiMol model, we recommend using conda for Python environment configuration. If you encounter any problems with the installation, please feel free to post an issue or discussion it.

Installing MiniConda (skip if conda was installed)

    wget https://repo.continuum.io/miniconda/Miniconda3-latest-Linux-x86_64.sh
    sh Miniconda3-latest-Linux-x86_64.sh

Creating GeminiMol environment

    conda create -n GeminiMol python=3.8.16
    conda activate GeminiMol

Setting up GeminiMol PATH and configuration

    git clone https://github.com/Wang-Lin-boop/GeminiMol
    cd GeminiMol/
    echo "# GeminiMol" >> ~/.bashrc
    echo "export PATH=\"${PWD}:\${PATH}\"" >> ~/.bashrc # optional, not required in the current version
    echo "export GeminiMol=\"${PWD}\"" >> ~/.bashrc
    source ~/.bashrc
    echo "export geminimol_app=\"${GeminiMol}/geminimol\"" >> ~/.bashrc # geminimol applications     
    echo "export geminimol_lib=\"${GeminiMol}/models\"" >> ~/.bashrc # geminimol models 
    echo "export geminimol_data=\"${GeminiMol}/data\"" >> ~/.bashrc # compound library
    source ~/.bashrc

Download datasets and models

In this repository, we provide the pre-trained GeminiMol and CrossEncoder models.

Download model parameters and weights via Google Driver and HuggingFace

Here is an example of how to download a model from huggingface. Besides wget, you can also download the model directly from Google Cloud Drive or huggingface using your browser.

git clone https://huggingface.co/AlphaMWang/GeminiMol    

Then, we need place the models to the ${GeminiMol}/models.

Download all chemical datasets via Zenodo for applications

    cd ${geminimol_data}
    wget https://zenodo.org/records/10450788/files/ChemDiv.zip # compound library for virtual screening
    wget https://zenodo.org/records/10450788/files/DTIDB.zip # DTI database for target identification 
    for i in Benchmark*.zip css*.zip Chem*.zip;do
        mkdir ${i%%.zip}
        unzip -d ${i%%.zip}/ $i
    done
    unzip -d compound_library/ ChemDiv.zip 
    unzip -d compound_library/ DTIDB.zip 

The expected structure of GeminiMol path is:

GeminiMol
├── geminimol                            # all code for GeminiMol and CrossEncoder
│   ├── model                            # code for GeminiMol and CrossEncoder models
│   │   ├── CrossEncoder.py              # model and methods for CrossEncoder     
│   │   ├── GeminiMol.py                 # model and methods for GeminiMol models  
│   ├── utils                            # utils in this work
│   │   ├── chem.py                      # basic tools for cheminformatics 
│   │   ├── dataset_split.py             # tools for dataset split 
│   │   ├── fingerprint.py               # basic tools for molecular fingerprints 
│   ├── Analyzer.py                      # analysis given molecules using presentation methods
│   ├── AutoQSAR.py                      # molecular proptery modeling by AutoGluon     
│   ├── PropDecoder.py                   # molecular proptery modeling by our PropDcoder
│   ├── FineTuning.py                    # molecular proptery modeling by fine-tune GeminiMol models
│   ├── Screener.py                      # screening molecules by GeminiMol similarity     
│   ├── CrossEncoder_Training.py         # scripts for training the CrossEncoders.
│   ├── GeminiMol_Training.py            # scripts for training the GeminiMol models.                 
│   ├── benchmark.py                     # benchmarking presentation methods on provide datasets
├── data                                 # training and benchmark datasets in this work
│   ├── Benchmark_DUD-E                  # virtual screeening benchmark, optional         
│   ├── Benchmark_LIT-PCBA               # virtual screeening benchmark, optional               
│   ├── Benchmark_TIBD                   # target identification benchmark, optional       
│   ├── Benchmark_QSAR                   # QSAR and ADMET benchmarks, optional           
│   ├── Chem_SmELECTRA                   # text backbone of chemical language, optional    
│   ├── css_library                      # CSS training data, optional   
│   ├── benchmark.json                   # dataset index for benchmark tasks, optional            
│   ├── database.csv                     # molecular datasets in this work, optional         
│   ├── compound_library                 # the compound librarys
│   │   ├── DTIDB.csv                    # dataset used in target identification    
│   │   ├── ChemDiv.csv                  # library of common commercial compounds     
│   │   ├── Specs.csv                    # library of common commercial compounds    
├── models                               # CrossEncoder and GeminiMol models
│   ├── CrossEncoder                     # CrossEncoder, optional                               
│   ├── GeminiMol                        # GeminiMol, recommended for zero-shot tasks   

Installing the dependency packages

Before running GeminiMol, you need to install the basic dependency packages.

Installing the RDkit for generating fingerprints

    pip install rdkit

Installing the statatics and plot packages

    pip install six
    pip install oddt scikit-learn matplotlib scipy==1.10.1

Installing the dependency packages of GeminiMol

    pip install torch==1.13.1+cu116 torchvision==0.14.1+cu116 \
        --extra-index-url https://download.pytorch.org/whl/cu116
    pip install dgl==1.1.1+cu116 -f https://data.dgl.ai/wheels/cu116/repo.html
    pip install dglgo==0.0.2 -f https://data.dgl.ai/wheels-test/repo.html
    pip install dgllife==0.3.2

If you intend to reproduce the benchmark results in our work, it is required to install the AutoGluon.

    pip install autogluon==0.8.1  # requried for AutoQSAR

📓 Application

As a molecular representation model, GeminiMol finds applications in ligand-based virtual screening, target identification, and quantitative structure-activity relationship (QSAR) modeling of small molecular drugs.

We have provided Cross-Encoder and GeminiMol models that can be used directly for inference. Here, we demonstrate the utilization of GeminiMol for virtual screening, target identification, and molecular property modeling.

Please note that while molecular fingerprints are considered simple molecular representation methods, they are an indispensable baseline (see our paper). When conducting your drug development project, we recommend exploring ECFP4, CombineFP, and GeminiMol that are provided simultaneously in our PharmProfiler.py and various molecular property modeling scripts.

Virtual Screening and Target Identification

In concept, molecules share similar conformational space also share similar biological activities, allowing us to predict the similarity of biological activities between molecules by comparing the similarity of GeminiMol encodings.

Here, we introduce the PharmProfiler.py, a novel approach that employs the GeminiMol encoding to establish pharmacological profiles and facilitate the search for molecules with specific properties in chemical space.

PharmProfiler.py offers the capability to conduct ligand-based virtual screening using commercially available compound libraries. Furthermore, it enables target identification through ligand similarity analysis by leveraging comprehensive drug-target relationship databases.

To support experimentation, we have included a collection of diverse commercial compound libraries and drug-target relationship databases, conveniently located in the ${geminimol_data}/compound_library/ directory.

1. Prepare the pharmacological profile and compound libraries

To define a pharmacological profile, you will need to input a profile.csv file, which should have the following format:

SMILES,Label
C=CC(=O)N[C@@H]1CN(c2nc(Nc3cn(C)nc3OC)c3ncn(C)c3n2)C[C@H]1F,1.0
C=CC(=O)Nc1cccc(Nc2nc(Nc3ccc(N4CCN(C(C)=O)CC4)cc3OC)ncc2C(F)(F)F)c1,1.0
C#Cc1cccc(Nc2ncnc3cc(OCCOC)c(OCCOC)cc23)c1,1.0
COC(=O)CCC/N=C1\SCCN1Cc1ccccc1,0.4
C=C(C)[C@@H]1C[C@@H](CC2(CC=C(C)C)C(=O)C(C(CC(=O)O)c3ccccc3)=C3O[C@@H](C)[C@@H](C)C(=O)C3=C2O)C1(C)C,-0.8
C/C(=C\c1ncccc1C)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1,-0.5

The "Label" column signifies the weight assigned to the reference compound. Positive values indicate that the selected compounds should bear resemblance to the reference compound, while negative values imply that the selected compounds should be dissimilar to the reference compound. Typically, positive values are assigned to active compounds, whereas negative values are assigned to inactive compounds or those causing side effects.

The compound libraries are also stored in CSV format in the ${geminimol_data}/compound_library/ directory. It is requried to maintain consistency between the SMILES column name in the profile.csv file and the compound library.

1. Perform the PharmProfiler

To perform virtual screening, the following command can be used.

Here, profile_set represents the provided pharmacological profile by the user, keep_top indicates the number of compounds to be outputted in the end, and probe_cluster determines whether compounds with the same weight should be treated as a cluster. Compounds within the same cluster will be compared individually with the query mol, and the highest similarity score will be taken as the score of query mol.

We have provided a processed version of the commercial Specs and ChemDiv compound library at the ${geminimol_data}/compound_library/specs.csv and ${geminimol_data}/compound_library/ChemDiv.csv, which contained 335,212 and 1,755,930 purchasable compounds.

export job_name="Virtual_Screening"
export profile_set="profile.csv" # SMILES (same to compound library) and Label (requried)
export compound_library="${geminimol_data}/compound_library/ChemDiv.csv" 
export smiles_column="SMILES" # Specify the column name in the compound_library
export weight_column="Label" # weights for profiles
export keep_top=1000
export probe_cluster="Yes"
python -u ${geminimol_app}/PharmProfiler.py "${geminimol_lib}/GeminiMol" "${job_name}" "${smiles_column}" "${compound_library}" "${profile_set}:${weight_column}" "${keep_top}"  "${probe_cluster}"

To perform target identification, the compound library can be replaced with the ${geminimol_data}/compound_library/DTIDB.csv, which contains drug-target relationships. This is a processed version of the BindingDB database, which contains 2,159,221 target-ligand paris.

export job_name="Target_Identification"
export profile_set="profile.csv" # Ligand_SMILES (same to compound library), and Label (requried)
export compound_library="${geminimol_data}/compound_library/DTIDB.csv" 
export smiles_column="SMILES" # Specify the column name in the compound_library
export weight_column="Label" # weights for profiles
export keep_top=2000
export probe_cluster="No"
python -u ${geminimol_app}/PharmProfiler.py "${geminimol_lib}/GeminiMol" "${job_name}" "${smiles_column}" "${compound_library}" "${profile_set}:${weight_column}" "${keep_top}"  "${probe_cluster}"

After the initial run of PharmProfiler, a extracted GeminiMol feature file will be generated in the ${geminimol_data}/compound_library/. Subsequent screening tasks on the same compound library can benefit from PharmProfiler automatically reading the feature file, which helps to accelerate the running speed.

Molecular Proptery Modeling (QSAR and ADMET)

1. Prepare your datasets

Before conducting molecular property modeling, it is crucial to carefully prepare your data, which includes compound structure pre-processing and dataset splitting.

Firstly, you need to clarify the chirality and protonation states of molecules in the dataset, which can be done using chemical informatics tools such as RDKit or Schrödinger software package. Typically, omitting pre-processing will not result in an error, but it may potentially impair the performance of GeminiMol.

The processed data should be saved in CSV file format, containing at least one column for SMILES and one column for Labels. Subsequently, utilize the following command for skeleton splitting. You can modify the script to change the splitting ratio, where by default, 70% of the dataset is used for training and 30% for validation and testing.

export dataset_path="data.csv"
export dataset_name="My_QSAR"
export smiles_column="SMILES" # Specify the column name in datasets
export label_column="Label" # Specify the column name in datasets
python -u ${geminimol_app}/utils/dataset_split.py "${dataset_path}" "${dataset_name}" "${smiles_column}" "${label_column}"
mkdir ${dataset_name}
mv ${dataset_name}_scaffold_*.csv ${dataset_name}/
export task=${dataset_name}

1. Training the molecular property prediction model

We have presented three approaches for molecular property modeling, namely AutoQSAR (broad applicability, slow speed), PropDecoder (fast speed), and FineTuning (optimal performance, moderate speed).

Given that you have enough experience with hyperparameter tuning, the attainment of optimal performance can be accomplished through the utilization of the FineTuning script to invoke GeminiMol. Also, AutoQSAR is recommended if you lack experience with hyperparameter tuning.

2.1 Fine-Tuning on downstream task

export task="Your_Dataset" # Specify a path to your datasets (train, valid, and test)
export smiles_column="SMILES" # Specify the column name in datasets
export label_column="Label" # Specify the column name in datasets
python -u ${geminimol_app}/FineTuning.py "${task}" "${geminimol_lib}/GeminiMol" "${smiles_column}" "${label_column}" "${task}_GeminiMol"

2.2 AutoQSAR (AutoGluon)

It is recommended to try using AutoQSAR to call CombineFP or GeminiMol when you lack deep learning experience, which usually produces a model with good performance.

export encoder_method="${geminimol_lib}/GeminiMol" # only GeminiMol

In our paper, we introduced a powerful joint molecular fingerprint baseline method named CombineFP.In our experiments, the performance of CombineFP in molecular property modeling is very superior and we highly recommend trying CombineFP along with GeminiMol.

export encoder_method="ECFP4:AtomPairs:TopologicalTorsion:FCFP6" # CombineFP

Having defined the encoder, you can train the model to convert the encoding of the molecule into properties using AutoQSAR. In fact, a potential advantage of this over FineTuning is that it can decode diverse molecular properties based on the fixed encoding, which will speed up the efficiency of chemical space searching.

export task="Your_Dataset" # Specify a path to your datasets (train, valid, and test)
export smiles_column="SMILES" # Specify the column name in datasets
export label_column="Label" # Specify the column name in datasets
python -u ${geminimol_app}/AutoQSAR.py "${task}" "${encoder_method}" "${smiles_column}" "${label_column}" "" "${task}_GeminiMol"

If the integration of molecular fingerprints and a pre-trained GeminiMol model is desired for training a molecular property prediction model, either PropDecoder or AutoQSAR can be employed.

export fingerprints="ECFP4:AtomPairs:TopologicalTorsion:FCFP6:MACCS" # CombineFP+MACCS
export encoder_method="${geminimol_lib}/GeminiMol:${fingerprints}" # CombineFP+MACCS+GeminiMol
export task="Your_Dataset" # Specify a path to your datasets (train, valid, and test)
export smiles_column="SMILES" # Specify the column name in datasets
export label_column="Label" # Specify the column name in datasets
python -u ${geminimol_app}/AutoQSAR.py "${task}" "${encoder_method}" "${smiles_column}" "${label_column}" "" "${task}_GMFP"

2.3 PropDecoder

For the most tasks, performing fine-tuning or using AutoQSAR will give pretty good performance in molecular property modeling, so you don't need to try PropDecoder unless the first two give poor performance.

export task="Your_Dataset" # Specify a path to your datasets (train, valid, and test)
export smiles_column="SMILES" # Specify the column name in datasets
export label_column="Label" # Specify the column name in datasets
python -u ${geminimol_app}/PropDecoder.py "${task}" "${encoder_method}" "${smiles_column}" "${label_column}" "${task}_GeminiMol"

1. Make predictions (only for AutoQSAR or fine-Tuned models)

Next, we can load the model trained based on AutoQSAR and FineTuning to predict molecular properties in a new dataset.

export model_path="QSAR_GeminiMol" # ${task}_GeminiMol when your build QSAR model
export encoder_method="${geminimol_lib}/GeminiMol" # Match to the encoders selected during QSAR model training
export extrnal_data="dataset.csv" # must contain the ${smiles_column}
export smiles_column="SMILES" # Specify the column name in datasets
export model_type="FineTuning" # FineTuning, PropDecoder, ['LightGBM', 'LightGBMLarge', 'LightGBMXT', 'NeuralNetTorch'] for AutoQSAR
python -u ${geminimol_app}/PropPredictor.py "${model_path}" "${encoder_method}" "${extrnal_data}" "${smiles_column}" "${model_type}"

If you have constructed a regression model using AutoQSAR, refer to the following command.

export model_path="QSAR_GeminiMol" # ${task}_GeminiMol when your build QSAR model
export encoder_method="${geminimol_lib}/GeminiMol" # Match to the encoders selected during QSAR model training
export extrnal_data="dataset.csv" # must contain the ${smiles_column}
export smiles_column="SMILES" # Specify the column name in datasets
export model_type="NeuralNetTorch" # ['LightGBM', 'LightGBMLarge', 'LightGBMXT', 'NeuralNetTorch'] for AutoQSAR
export task_type="regression"
python -u ${geminimol_app}/PropPredictor.py "${model_path}" "${encoder_method}" "${extrnal_data}" "${smiles_column}" "${model_type}" "${task_type}"

Molecular Clustering

You can use GeminiMol to cluster molecules just like molecular fingerprints!

export encoder_method="${geminimol_lib}/GeminiMol" # Match to the encoders selected during QSAR model training
export data_table="dataset.csv" # must contain the ${smiles_column}
export smiles_column="SMILES" # Specify the column name in datasets
export output_fn="Cluster"
export cluster_num=10 # only for supervised clustering algorithm, such as K-Means
python -u ${geminimol_app}/Analyzer.py "${data_table}" "${encoder_method}" "${smiles_column}" "${output_fn}" "cluster:${cluster_num}"

Extract Molecular Features (GeminiMol Encoding)

You can use GeminiMol or molecular fingerprints to extract molecular features for further analysis.

export encoder_method="${geminimol_lib}/GeminiMol" # Match to the encoders selected during QSAR model training
export data_table="dataset.csv" # must contain the ${smiles_column}
export smiles_column="SMILES" # Specify the column name in datasets
export output_fn="${data_table%%.*}_Encoding"
python -u ${geminimol_app}/Analyzer.py "${data_table}" "${encoder_method}" "${smiles_column}" "${output_fn}" "encode"

👐 Reproducing

Here, we present the reproducible code for training the Cross-Encoder and GeminiMol models based on the CSS descriptors of 39,290 molecules described in the paper.

Download Training and Benchmark Datasets

Download all datasets via Zenodo for training, test and benchmark

    cd ${geminimol_data}
    wget https://zenodo.org/records/10450788/files/css_library.zip # only for reproducing GeminiMol training
    wget https://zenodo.org/records/10450788/files/Benchmark_DUD-E.zip # only for reproducing benchmark
    wget https://zenodo.org/records/10450788/files/Benchmark_LIT-PCBA.zip # only for reproducing benchmark
    wget https://zenodo.org/records/10450788/files/Benchmark_QSAR.zip # only for reproducing benchmark
    wget https://zenodo.org/records/10450788/files/Benchmark_TIBD.zip # only for reproducing benchmark
    wget https://zenodo.org/records/10450788/files/Chem_SmELECTRA.zip # only for reproducing cross-encoder baseline

Re-training our models

Training the Cross-Encoder

conda activate GeminiMol
export model_name="CrossEncoder"
export batch_size_per_gpu=200 # batch size = 200 (batch_size_per_gpu) * 4 (gpu number)
export epoch=20 # max epochs
export lr="1.0e-3" # learning rate
export label_list="MCMM1AM_MAX:LCMS2A1Q_MAX:MCMM1AM_MIN:LCMS2A1Q_MIN" # ShapeScore:ShapeAggregation:ShapeOverlap:CrossSim:CrossAggregation:CrossOverlap
CUDA_VISIBLE_DEVICES=0,1,2,3 python ${geminimol_app}/CrossEncoder_Training.py  "${geminimol_data}/css_library/" "${geminimol_data}/Chem_SmELECTRA"  "${epoch}"  "${lr}"  "${batch_size_per_gpu}"  "${model_name}"  "${geminimol_data}/benchmark.json" "${label_list}"

Training the GeminiMol Encoder and Decoder of CSS descriptors

conda activate GeminiMol
export model_name="GeminiMol"
export batch_size=512
export epoch=20 # max epochs
export patience=50 # for early stoping
export GNN='WLN' # Weisfeiler-Lehman Network (WLN)
export network="MeanMLP:2048:4:2048:None:0:5:0"
export label_dict="ShapeScore:0.2,ShapeAggregation:0.2,ShapeOverlap:0.05,ShapeDistance:0.05,CrossSim:0.15,CrossAggregation:0.15,CrossDist:0.05,CrossOverlap:0.05,MCS:0.1"
CUDA_VISIBLE_DEVICES=0 python -u ${geminimol_app}/GeminiMol_Training.py "${geminimol_data}/css_library/" "${epoch}" "${batch_size}" "${GNN}" "${network}" "${label_dict}" "${model_name}" "${patience}" "${geminimol_data}/benchmark.json" 

Benchmarking the fingerprints and our models

Additionally, benchmark test scripts were provided. With this code, the community can reproduce the results reported in the paper, explore different model architectures, even incorporate additional molecular similarity data to further enhance the performance of the models.

Benchmarking molecular fingerprints and GeminiMol on virutual screening and target identification

For each molecular fingerprint, we used all supported similarity metrics, including Tanimoto, Cosine, and Tversky. For the GeminiMol model, in addition to the projected heads used in pre-training, we introduced similarities between molecular representation vectors, including Cosine and Pearson. It is worth noting that in practice we cannot be sure which combination of molecular fingerprints and similarity metrics is optimal, and therefore each combination is considered an independent method in benchmarking.

conda activate GeminiMol
# benchmarking Fixed GeminiMol models and Fingerprints
for task in "DUDE" "LIT-PCBA" "TIBD" # zero-shot tasks
    do
for model_name in "FCFP6" "MACCS" "RDK" "ECFP6" "FCFP4" \
    "TopologicalTorsion" "AtomPairs" "ECFP4" \
    "${geminimol_lib}/GeminiMol"
    do
mkdir -p ${model_name}
CUDA_VISIBLE_DEVICES=0 python -u ${geminimol_app}/benchmark.py "${model_name}" "${geminimol_data}/benchmark.json"  "${task}"
done
done

Benchmarking molecular fingerprints and GeminiMol on molecular property modeling

It is worth noting that different decoders exhibit varying performance on different tasks and encodings. Therefore, it is essential to select the appropriate decoder for each specific molecular encoder and task. In practice, we can determine when the model should stop-training and choose the optimal decoder architecture by dividing the training, validation and test sets. Consequently, all results should be merged using a data pivot table to analyze the optimal decoder for each encoder-task combination. In our work, the hyperparameters of the PropDecoder were chosen based on empirical experience and were not subjected to any hyperparameter tuning. Performing further hyperparameter tuning for each task may potentially yield improved performance.

for task in "ADMET-C" "ADMET-R" \
    "LIT-QSAR" "CELLS-QSAR" "ST-QSAR" "PW-QSAR" \
    "PropDecoder-ADMET" "PropDecoder-QSAR" # fixed the molecular encoder
    do
for model_name in "CombineFP" \
    "FCFP6" "MACCS" "RDK" "ECFP6" "FCFP4" "TopologicalTorsion" "AtomPairs" "ECFP4" \
    "${geminimol_lib}/GeminiMol"
    do
mkdir -p ${model_name}
CUDA_VISIBLE_DEVICES=0 python -u ${geminimol_app}/benchmark.py "${model_name}" "${geminimol_data}/benchmark.json"  "${task}"
done
done
for task in "FineTuning-ADMET" "FineTuning-QSAR"; do # benchmarking with FineTuning GeminiMol models
for model_name in "${geminimol_lib}/GeminiMol"; do
CUDA_VISIBLE_DEVICES=0 python -u ${geminimol_app}/benchmark.py "${model_name}" "${geminimol_data}/benchmark.json"  "${task}"
done
done

⭐ Citing This Work

Conformational Space Profile Enhances Generic Molecular Representation Learning
Lin Wang, Shihang Wang, Hao Yang, Shiwei Li, Xinyu Wang, Yongqi Zhou, Siyuan Tian, Lu Liu, Fang Bai
bioRxiv 2023.12.14.571629; doi: https://doi.org/10.1101/2023.12.14.571629

✅ License

GeminiMol is released under the Academic Free Licence, which permits academic use, modification and distribution free of charge. GeminiMol can be utilized in academic publications, open-source software projects, and open-source competitions (e.g. Kaggle competitions under the MIT Open Source license).

GeminiMol prohibits unauthorised commercial use, including commercial training and as part of a paid computational platform, which intended to prevent speculators from exploiting informational asymmetry for profit. Communication and authorization with our supervisor is permitted for its application in pipeline development and research activities within pharmaceutical R&D.

💌 Get in Touch

We welcome community contributions of extension tools based on the GeminiMol model, etc. If you have any questions not covered in this overview, please contact the GeminiMol Developer Team. We would like to hear your feedback and understand how GeminiMol has been useful in your research. Share your stories with us.

😃 Acknowledgements

We appreciate the technical support provided by the engineers of the high-performance computing cluster of ShanghaiTech University. Lin Wang also thanks Jianxin Duan, Gaokeng Xiao, Quanwei Yu, Zheyuan Shen, Shenghao Dong, Huiqiong Li, Zongquan Li, and Fenglei Li for providing technical support, inspiration and help for this work. We express our gratitude to Dr. Zhongji Pu, Dr. Quanwei Yu for their invaluable assistance in third-party testing for model installation, reproducibility and application.

We also thank the developers and maintainers of MarcoModel and PhaseShape modules in the Schrödinger package. Besides, GeminiMol communicates with and/or references the following separate libraries and packages, we thank all their contributors and maintainers!

• RDKit
• PyTorch
• AutoGluon
• DGL-Life
• ODDT
• SciPy
• scikit-learn
• matplotlib