--- license: cc-by-nc-sa-4.0 configs: - config_name: default data_files: - split: HCT116 path: "data/HCT116*.parquet" - split: HEK293T path: "data/HEK293T*.parquet" - config_name: gene_metadata data_files: metadata/gene_metadata.parquet --- # X-Atlas/Orion X-Atlas: Orion edition (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. Through the release of X-Atlas/Orion, we highlight the potential of FiCS Perturb-seq to address current scalability and variability challenges in data generation, advance foundation model development that incorporates gene-dosage effects, and accelerate biological discoveries. **Preprint**: [X-Atlas/Orion: Genome-wide Perturb-seq Datasets via a Scalable Fix-Cryopreserve Platform for Training Dose-Dependent Biological Foundation Models](https://www.biorxiv.org/content/10.1101/2025.06.11.659105v1)
**Processed h5ads and other metadata**: https://doi.org/10.25452/figshare.plus.29190726 ## Tutorial ```python from datasets import load_dataset # load the entire dataset in streaming mode ds = load_dataset("Xaira-Therapeutics/X-Atlas-Orion", streaming=True) # load only hct116 hct116_ds = load_dataset("Xaira-Therapeutics/X-Atlas-Orion", streaming=True, split="HCT116") # load only hek293t hek293t_ds = load_dataset("Xaira-Therapeutics/X-Atlas-Orion", streaming=True, split="HEK293T") ``` ## Dataset The dataset contains the following information: | **name** | **description** | |------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------| | `gene_token_id` | gene identifiers corresponding to genes with non-zero expression in each cell. to be used with `gene_expression`.
`metadata/gene_metadata.parquet` contains the mapping from `gene_token_id` to Ensembl ID and official gene symbol | | `gene_expression` | raw counts for genes with non-zero expression. to be used with `gene_token_id` | | `cell_barcode` | 10X-generated cell barcode. the suffix `-1` is replaced with `-` | | `sample` | GEM batch | | `num_features` | number of guides | | `guide_target` | guide identity | | `gene_target` | gene targeted by guide | | `n_genes_by_counts` | number of genes with non-zero counts | | `total_counts` | total UMIs | | `total_counts_mt` | total UMIs from MT genes | | `pct_counts_mt` | % UMIs from MT genes | | `pass_guide_filter` | boolean if cells contains two guides from the same guide pair | ## Gene metadata All samples were aligned to the 10x Genomics GRCh38 2024-A pre-built reference genome ([human reference (GRCh38) - 2024-A](https://www.10xgenomics.com/support/software/cell-ranger/downloads#reference-downloads)). Official gene symbols and ensembl IDs were extracted from the `genes.gtf` file. ```python # load metadata containing mappings to gene tokens and names gene_metadata = load_dataset("Xaira-Therapeutics/X-Atlas-Orion","gene_metadata") ``` | name | description | |---------------|------------------------------------------------------------------------------------------------------| | `ensembl_id` | Ensembl ID | | `gene_name` | official gene symbol | | `gene_token_id` | gene identifiers corresponding to genes with non-zero expression in each cell. to be used with `gene_token_id` in the dataset | ## 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} } ```