Datasets:
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license: cc-by-4.0
pretty_name: MultiOmics_GS-LGG
task_categories:
- tabular-classification
tags:
- tabular
- biomedical
- benchmark
- TabBioMed
- systems-biology
- classification
size_categories:
- n<1K
configs:
- config_name: default
data_files:
- split: fold_0_train
path: data/fold_0/train.parquet
- split: fold_0_validation
path: data/fold_0/val.parquet
- split: fold_0_test
path: data/fold_0/test.parquet
- split: fold_1_train
path: data/fold_1/train.parquet
- split: fold_1_validation
path: data/fold_1/val.parquet
- split: fold_1_test
path: data/fold_1/test.parquet
- split: fold_2_train
path: data/fold_2/train.parquet
- split: fold_2_validation
path: data/fold_2/val.parquet
- split: fold_2_test
path: data/fold_2/test.parquet
- split: fold_3_train
path: data/fold_3/train.parquet
- split: fold_3_validation
path: data/fold_3/val.parquet
- split: fold_3_test
path: data/fold_3/test.parquet
- split: fold_4_train
path: data/fold_4/train.parquet
- split: fold_4_validation
path: data/fold_4/val.parquet
- split: fold_4_test
path: data/fold_4/test.parquet
MultiOmics_GS-LGG
Part of TabBioMed (TabBioMed: A Large-Scale Benchmark for Biomedical Tabular Learning), a benchmark of 94 curated biomedical tabular datasets. Code, preprocessing and documentation: https://github.com/AI-sandbox/TabBioMed.
TCGA lower-grade glioma three-class classification, with 247 distinct patients. CNV (5,000), mRNA (3,435) and miRNA (102) features and targets are retained from MLOmics. DNA methylation is reconstructed from TCGA/Xena HumanMethylation450 by verified CpG identifiers and primary-tumour patient barcodes: 4,705 of the 5,000 original probes are assayed; the 295 unassayed probes are excluded. Missing beta values remain missing for fold-fitted imputation. Existing five outer folds and three-fold inner CV are retained. Patient identifiers are metadata, never features.
| Domain | Task | Samples | Features | Classes |
|---|---|---|---|---|
| Systems Biology | classification | 247 | 13,242 | 3 |
Splits. 5 stored outer cross-validation folds (data/fold_<i>/), each with train/val/test files (fold 0: 172/25/50 rows). Every row appears in exactly one outer test fold. HPO in the paper uses inner folds drawn from each outer non-test pool.
Files
data/**.parquet: one row per sample.row_idxis the row index in the original TabBioMed array;f_<i>[_<name>]are the features (in order);target(ortarget_<j>for multi-target tasks) is the label. Categorical feature indices (0-based, among the features):[]. Missing values are stored as nulls.metadata.json: TabBioMed task metadata (task type, categorical indices, source, description).feature_names.json: original feature names, in column order.sample_metadata.csv: per-row provenance (identifiers, source annotations); not features.
from datasets import load_dataset
ds = load_dataset("TabBioMed/MultiOmics_GS-LGG")
A Croissant (1.1) description with Responsible-AI fields is distributed with the TabBioMed release.
Source and license
Source: MLOmics GS-LGG with TCGA/Xena HumanMethylation450
This derived dataset is distributed under CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/). Please also cite and respect the terms of the original source.
Citation
@inproceedings{tabbiomed2026,
title = {TabBioMed: A Large-Scale Benchmark for Biomedical Tabular Learning},
author = {Mateo Bernad{\'o}, Pau and Polapragada, Saivenkata Nagavyjayanthi and Bonet, David and Arbiol Rakuljic, Pol and Mogas Pladevall, Laia and Comajoan Cara, Mar{\c{c}}al and Gonzalez Ferrer, Jesus and Abante, Jordi and Mas Montserrat, Daniel and Haussler, David and Ioannidis, Alexander G.},
booktitle = {Advances in Neural Information Processing Systems (NeurIPS), Evaluations and Datasets Track},
year = {2026}
}