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---
dataset_info:
features:
- name: seq
dtype: string
- name: 'y'
dtype: float64
splits:
- name: train
num_bytes: 20823
num_examples: 248
- name: val
num_bytes: 4422
num_examples: 53
- name: test
num_bytes: 4545
num_examples: 54
download_size: 12650
dataset_size: 29790
configs:
- config_name: default
data_files:
- split: train
path: data/train-*
- split: val
path: data/val-*
- split: test
path: data/test-*
license: mit
---
πŸ“Š **Tc-Riboswitch Dataset**
This dataset contains synthetic tetracycline (Tc) riboswitches along with their functional performance metrics.
It's a curated resource for training machine learning models to predict gene expression from RNA sequences.
The original dataset is from CodonBERT.
⁉️ **Dataset Contents**
- Sequence: The mRNA sequence of the synthetic riboswitch.
- Switching_factor: A numerical value that quantifies the riboswitch's regulatory effect.
This value represents the change in gene expression in the presence versus the absence of tetracycline.
🎯 **Purpose**
This dataset serves as a benchmark for fine-tuning models on a **regression task**, predicting riboswitch behavior from its sequence.
We used this dataset to fine-tune **CDS-BART**, a BART-based foundation model trained on massive mRNA sequences.
Demonstrating its ability to perform downstream tasks related to mRNA regulation which are fine-tuned for various mRNA-related downstream task.
**CDS-BART** available at [GitHub](https://github.com/mogam-ai/CDS-BART)
πŸ”§**Usage**
```python
from datasets import load_dataset
dataset = load_dataset('mogam-ai/CDS-BART-Tc-Riboswitches')
```
πŸ“š **Dataset Reference**
- Groher, Ann-Christin, et al. "Tuning the performance of synthetic riboswitches using machine learning." *ACS Synthetic Biology* 8.1 (2018): 34-44.
- Li, Sizhen, et al. "CodonBERT large language model for mRNA vaccines." Genome research 34.7 (2024): 1027-1035.