--- viewer: true license: cc-by-nc-sa-4.0 configs: - config_name: HEK293T-cells data_dir: "data/HEK293T/cells.lance" - config_name: HEK293T-expression data_dir: "data/HEK293T/expression.lance" - config_name: HEK293T-genes data_dir: "data/HEK293T/genes.lance" - config_name: HCT116-cells data_dir: "data/HCT116/cells.lance" - config_name: HCT116-expression data_dir: "data/HCT116/expression.lance" - config_name: HCT116-genes data_dir: "data/HCT116/genes.lance" language: - en tags: - biology - genomics - RNA - single-cell - lance - slaf pretty_name: X-Atlas-Orion --- # X-Atlas Orion Dataset (SLAF Format) ## Attribution **This is a re-release of data originally generated by [Xaira Therapeutics](https://huggingface.co/Xaira-Therapeutics).** - **Original Dataset**: [Xaira-Therapeutics/X-Atlas-Orion](https://huggingface.co/datasets/Xaira-Therapeutics/X-Atlas-Orion) - **Original Format**: Parquet files - **This Release**: Same data in SLAF (Sparse Lazy Array Format) - **License**: CC-BY-NC-SA-4.0 (Creative Commons Attribution-NonCommercial-ShareAlike 4.0) - **Original Citation**: ``` @article{huang2025xatlasorion, title={X-Atlas/Orion: Genome-wide Perturb-seq Datasets via a Scalable Fix-Cryopreserve Platform for Training Dose-Dependent Biological Foundation Models}, author={Huang, Ann C and Hsieh, Tsung-Han S and Zhu, Jiang and Michuda, Jackson and Teng, Ashton and Kim, Soohong and Rumsey, Elizabeth M and Lam, Sharon K and Anigbogu, Ikenna and Wright, Philip and Ameen, Mohamed and You, Kwontae and Graves, Christopher J and Kim, Hyunsung John and Litterman, Adam J and Sit, Rene V and Blocker, Alex and Chu, Ci}, journal={bioRxiv}, year={2025}, url={https://www.biorxiv.org/content/10.1101/2025.06.11.659105v1} } ``` For detailed information about the dataset, methodology, and original publication, please refer to the [original dataset repository](https://huggingface.co/datasets/Xaira-Therapeutics/X-Atlas-Orion). ## Dataset Description X-Atlas/Orion is a Perturb-seq atlas containing two genome-wide Fix-Cryopreserve-ScRNAseq (FiCS) Perturb-seq screens that target all human protein-coding genes (n = 18,903 genes). The dataset is comprised of eight million HCT116 and HEK293T cells, each deeply sequenced to a median of 16,000 unique molecular identifiers (UMIs) per cell. The median on-target knockdown efficiency is 75.4% in HCT116 cells and 51.5% in HEK293T cells, with a median of at least 140 cells per perturbation. This release provides the same data in SLAF format for compatibility with SLAF tools. For more detailed information, see the [original dataset repository](https://huggingface.co/datasets/Xaira-Therapeutics/X-Atlas-Orion). ## Usage This dataset is in [SLAF (Sparse Lazy Array Format)](https://slaf-project.github.io/slaf/) format, which uses the [Lance](https://lance.org/) table format for storage. You can use it with the `slafdb` library (for SLAF format), or `pylance` library (for direct Lance access). ### Using SLAF (Recommended for SLAF Format) ```bash pip install slafdb ``` ```python hf_path = 'hf://datasets/slaf-project/X-Atlas-Orion' from slaf import SLAFArray slaf_hct116 = SLAFArray(f"{hf_path}/data/HCT116") slaf_hct116.query("SELECT * FROM cells LIMIT 10") ``` ### Using Lance Directly ```bash pip install pylance ``` ```python hf_path = 'hf://datasets/slaf-project/X-Atlas-Orion' import lance lance_hct116_ds = lance.dataset(f"{hf_path}/data/HCT116/cells.lance") lance_hct116_ds.sample(10) ```