AlphaGenome / README.md
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---
license: apache-2.0
tasks:
- genomic-sequence-modeling
frameworks:
- jax
language:
- en
- zh
tags:
- OneScience
- Life Sciences
- Genomics
- DNA Sequence Model
- Variant Effect Prediction
- AlphaGenome
datasets:
- OneScience/alphagenome_dataset
---
<p align="center">
<strong>
<span style="font-size: 30px;">AlphaGenome</span>
</strong>
</p>
# Model Introduction
AlphaGenome is a DNA sequence model proposed by Google DeepMind. It can take DNA intervals up to 1 Mbp as input and predict multiple classes of genomic functional signals for track prediction and regulatory variant effect scoring.
Paper: Advancing regulatory variant effect prediction with AlphaGenome
https://www.nature.com/articles/s41586-025-10014-0
# Model Description
AlphaGenome is implemented based on JAX / Flax and supports genomic interval inference, variant effect scoring, track evaluation, and fine-tuning examples. This model package is accompanied by the ModelScope dataset `OneScience/alphagenome_dataset`, which can be used for quick local verification.
# Applicable Scenarios
| Scenario | Description |
| :---: | :--- |
| Genomic interval prediction | Input a reference genome FASTA, chromosome, and interval coordinates, and output predicted tracks for ATAC, DNase, CAGE, RNA-seq, ChIP, and other signals |
| Variant effect scoring | Input a VCF or built-in example variants, compare prediction differences between reference and variant sequences, and generate a variant scoring table |
| Track prediction evaluation | Use validation data from the AlphaGenome dataset to calculate regression evaluation metrics for different assay bundles |
| Fine-tuning experiments | Use a custom reference genome, interval CSV, and BigWig signal files to verify the fine-tuning workflow |
| ModelScope / OneCode runtime | After downloading the model project and accompanying dataset, quickly verify script connectivity in a biology-domain runtime environment |
# Usage Instructions
## 1. OneCode Usage
You can experience intelligent one-click AI4S programming through the OneCode online environment:
[Click to experience intelligent one-click AI4S programming](https://web-2069360198568017922-iaaj.ksai.scnet.cn:58043/home)
## 2. Manual Installation and Usage
**Hardware Requirements**
- GPU or DCU runtime is recommended.
- CPU can be used for import checks and small-configuration connectivity verification, but full training and inference are slow.
- DCU users need to install DTK in advance. DTK 25.04.2 or later is recommended, or the OneScience-recommended version matching the current cluster.
**Environment Check**
- NVIDIA GPU:
```bash
nvidia-smi
```
- Hygon DCU:
```bash
hy-smi
```
### Download the Model Package
```bash
modelscope download --model OneScience/alphagenome --local_dir ./alphagenome
cd alphagenome
```
### Install the Runtime Environment
**DCU Environment**
```bash
# First activate DTK and Conda
conda create -n onescience311 python=3.11 -y
conda activate onescience311
# Supports uv installation
pip install onescience[bio-dcu] -i http://mirrors.onescience.ai:3141/pypi/simple/ --trusted-host mirrors.onescience.ai
```
After installation, return to the model package directory:
```bash
cd ./alphagenome
```
### Training and Inference Data Introduction
The OneScience community has uploaded the data required for AlphaGenome inference, evaluation, and fine-tuning to ModelScope: [OneScience/alphagenome_dataset](https://modelscope.cn/datasets/OneScience/alphagenome_dataset). After downloading, place the data in the `data/` directory of the model package.
```bash
modelscope download --dataset OneScience/alphagenome_dataset --local_dir ./data
```
### Training Weights
The repository includes `weight/alphagenome-all-folds`, and all scripts also support specifying model weights through `--model_dir`.
### Prepare Weights
If using local weights, place the AlphaGenome Orbax checkpoint in the following directory:
```text
weight/
alphagenome-all-folds/
_CHECKPOINT_METADATA
_METADATA
...
```
If running in a shared runtime environment, you can also reuse a unified directory through environment variables:
```bash
export ONESCIENCE_MODELS_DIR=/path/to/onescience/models
export ONESCIENCE_DATASETS_DIR=/path/to/onescience/datasets
```
The scripts will preferentially read:
- `${ONESCIENCE_MODELS_DIR}/AlphaGenome/alphagenome-all-folds`
- `${ONESCIENCE_DATASETS_DIR}/AlphaGenome`
If the above environment variables are not set, the defaults under the current model package are read:
- `weight/alphagenome-all-folds`
- `data/`
### Interval Inference
```bash
bash scripts/inference.sh
```
Equivalent Python command example:
```bash
python scripts/run_inference.py \
--fasta_path ./data/reference/HOMO_SAPIENS/GRCh38.p13.genome.fa \
--model_dir ./weight/alphagenome-all-folds \
--chromosome chr19 \
--start 10587331 \
--end 11635907 \
--output_dir ./outputs
```
Inference results will be saved to `outputs/`.
### Variant Effect Scoring
```bash
bash scripts/run_variant.sh
```
When specifying VCF input, you can use:
```bash
python scripts/run_variant_scoring.py \
--vcf_path ./data/example.vcf \
--fasta_path ./data/reference/HOMO_SAPIENS/GRCh38.p13.genome.fa \
--model_dir ./weight/alphagenome-all-folds \
--output_dir ./outputs_variant
```
Scoring results will be saved as CSV files.
### Track Prediction Evaluation
```bash
bash scripts/run_track.sh
```
You can also explicitly specify the data and output paths:
```bash
python scripts/run_track_prediction_eval.py \
--model_dir ./weight/alphagenome-all-folds \
--model_version ALL_FOLDS \
--data_dir ./data/v1/train \
--output_path ./outputs_track/eval_results.csv
```
### Fine-tuning Example
```bash
python scripts/run_finetuning.py \
--fasta_path ./data/reference/HOMO_SAPIENS/GRCh38.p13.genome.fa \
--regions_csv ./data/finetune_regions.csv \
--bigwig_paths ./data/sample_atac.bw \
--output_dir ./finetuned_model \
--num_steps 1000 \
--batch_size 2
```
# Data Format
The ModelScope dataset `OneScience/alphagenome_dataset` is recommended to be downloaded to `data/` under the model package. The default structure is as follows:
```text
data/
reference/
HOMO_SAPIENS/
GRCh38.p13.genome.fa
GRCh38.p13.genome.fa.fai
v1/
train/
...
```
Where:
- `reference/HOMO_SAPIENS/GRCh38.p13.genome.fa` is the human reference genome FASTA.
- `.fai` is the FASTA index file.
- `v1/train/` is the data directory used for track prediction evaluation.
- Custom fine-tuning also requires preparing an interval CSV file with column names `chromosome,start,end`, as well as one or more BigWig signal files.
# Official OneScience Information
| Platform | OneScience Main Repository | Skills Repository |
| --- | --- | --- |
| Gitee | https://gitee.com/onescience-ai/onescience | https://gitee.com/onescience-ai/oneskills |
| GitHub | https://github.com/onescience-ai/OneScience | https://github.com/onescience-ai/oneskills |
# Citations and License
- This repository is based on the AlphaGenome open-source model and provides DCU adaptation. The related source code uses the Apache License 2.0.
- For scientific research, cite the original paper: [Advancing regulatory variant effect prediction with AlphaGenome](https://www.nature.com/articles/s41586-025-10014-0).