metadata

version: 1.0.0
language: en
license: cc-by-4.0
source_datasets: curated
task_categories:
  - tabular-classification
  - tabular-regression
tags:
  - chemistry
  - cheminformatics
pretty_name: Mutagenicity Optimization
dataset_summary: >-
  The mutagenicity dataset consists of a training set with 6862 molecules and a
  test set with 1714 molecules.  The train and test datasets were created after
  sanitizing and splitting the original dataset in the paper below.
  Additionally, there is a validation dataset containing 1469 molecules that
  were not involved in the training set.
citation: |-
  @article {,
     author  = {Lou, C., Yang, H., Deng, H. et al.},
     title   = {Chemical rules for optimization of chemical mutagenicity via matched molecular pairs analysis and machine learning methods},
     journal = {Journal of Cheminformatics},
     year    = {2023},
     volume  = {15},
     number  = {35}
  }
size_categories:
  - 10K<n<100K
config_names:
  - train_test
  - validation
configs:
  - config_name: train_test
    data_files:
      - split: train
        path: train_test/train.csv
      - split: test
        path: train_test/test.csv
  - config_name: validation
    data_files:
      - split: validation
        path: validation/validation.csv
dataset_info:
  - config_name: train_test
    features:
      - name: SMILES
        dtype: string
      - name: ID
        dtype: int64
      - name: 'Y'
        dtype: int64
        description: >-
          Binary classification where 'O' represents 'non-mutagenic' and '1'
          represents 'mutagenic'
      - name: MW
        dtype: float64
    splits:
      - name: train
        num_bytes: 219712
        num_examples: 6862
      - name: test
        num_bytes: 54976
        num_examples: 1714
  - config_name: validation
    features:
      - name: SMILES
        dtype: string
      - name: 'Y'
        dtype: int64
        description: >-
          Binary classification where 'O' represents 'non-mutagenic' and '1'
          represents 'mutagenic'

Mutagenicity Optimization (MutagenLou2023)

In the original paper, they collected the Ames records from Hansen’s benchmark (6512 compounds) and the ISSSTY database (6052 compounds). After data preparation, a total of 8576 compounds with structural diversity were obtained, including 4643 Ames positives and 3933 Ames negatives. The comprehensive data set was then split into a training set including 7720 compounds and a test set containing 856 compounds. Overall, the numbers of negatives and positives in this data set were balanced with a ratio of 0.847 (Neg./Pos.). In addition, 805 approved drugs from DrugBank that were not involved in the training set, and 664 Ames strong positive samples from DGM/NIHS were built as an external validation set.

This is a mirror of the official Github repo where the dataset was uploaded in 2023.

Data splits

Here we have used the Realistic Split method described in (Martin et al., 2018) to split the MutagenLou2023 dataset.

Quickstart Usage

Load a dataset in python

Each subset can be loaded into python using the Huggingface datasets library. First, from the command line install the datasets library

$ pip install datasets

then, from within python load the datasets library

>>> import datasets

and load one of the MutagenLou2023 datasets, e.g.,

>>> train_test = datasets.load_dataset("maomlab/MutagenLou2023", name = "train_test")
Downloading readme: 100%|██████████|  7.15k/7.15k [00:00<00:00, 182kB/s]
Downloading data: 100%|██████████| 306k/306k [00:00<00:00, 4.45MkB/s]
Downloading data: 100%|██████████| 115k/115k [00:00<00:00, 668kkB/s]
Generating train split: 100%|██████████| 6862/6862 [00:00<00:00, 70528.05examples/s]
Generating test split: 100%|██████████| 1714/1714 [00:00<00:00, 22632.33 examples/s]

and inspecting the loaded dataset

>>> train_test
DatasetDict({
train: Dataset({
    features: ['SMILES', 'ID', 'Y', 'MW'],
    num_rows: 6862
})
test: Dataset({
    features: ['SMILES', 'ID', 'Y', 'MW'],
    num_rows: 1714
})
})

Use a dataset to train a model

One way to use the dataset is through the MolFlux package developed by Exscientia. First, from the command line, install MolFlux library with catboost and rdkit support

pip install 'molflux[catboost,rdkit]'

then load, featurize, split, fit, and evaluate the a catboost model

import json
from datasets import load_dataset
from molflux.datasets import featurise_dataset
from molflux.features import load_from_dicts as load_representations_from_dicts
from molflux.splits import load_from_dict as load_split_from_dict
from molflux.modelzoo import load_from_dict as load_model_from_dict
from molflux.metrics import load_suite

split_dataset = load_dataset('maomlab/MutagenLou2023', name = 'train_test')

split_featurised_dataset = featurise_dataset(
  split_dataset,
  column = "SMILES",
  representations = load_representations_from_dicts([{"name": "morgan"}, {"name": "maccs_rdkit"}]))

model = load_model_from_dict({
    "name": "cat_boost_classifier",
    "config": {
        "x_features": ['SMILES::morgan', 'SMILES::maccs_rdkit'],
        "y_features": ['Y']}})

model.train(split_featurised_dataset["train"])

preds = model.predict(split_featurised_dataset["test"])

classification_suite = load_suite("classification")

scores = classification_suite.compute(
    references=split_featurised_dataset["test"]['Y'],
    predictions=preds["cat_boost_classifier::Y"])

Citation

TY - JOUR AU - Lou, Chaofeng AU - Yang, Hongbin AU - Deng, Hua AU - Huang, Mengting AU - Li, Weihua AU - Liu, Guixia AU - Lee, Philip W. AU - Tang, Yun PY - 2023 DA - 2023/03/20 TI - Chemical rules for optimization of chemical mutagenicity via matched molecular pairs analysis and machine learning methods JO - Journal of Cheminformatics SP - 35 VL - 15 IS - 1 AB - Chemical mutagenicity is a serious issue that needs to be addressed in early drug discovery. Over a long period of time, medicinal chemists have manually summarized a series of empirical rules for the optimization of chemical mutagenicity. However, given the rising amount of data, it is getting more difficult for medicinal chemists to identify more comprehensive chemical rules behind the biochemical data. Herein, we integrated a large Ames mutagenicity data set with 8576 compounds to derive mutagenicity transformation rules for reversing Ames mutagenicity via matched molecular pairs analysis. A well-trained consensus model with a reasonable applicability domain was constructed, which showed favorable performance in the external validation set with an accuracy of 0.815. The model was used to assess the generalizability and validity of these mutagenicity transformation rules. The results demonstrated that these rules were of great value and could provide inspiration for the structural modifications of compounds with potential mutagenic effects. We also found that the local chemical environment of the attachment points of rules was critical for successful transformation. To facilitate the use of these mutagenicity transformation rules, we integrated them into ADMETopt2 (http://lmmd.ecust.edu.cn/admetsar2/admetopt2/), a free web server for optimization of chemical ADMET properties. The above-mentioned approach would be extended to the optimization of other toxicity endpoints. SN - 1758-2946 UR - https://doi.org/10.1186/s13321-023-00707-x DO - 10.1186/s13321-023-00707-x ID - Lou2023 ER -