crc-atlas

Single-cell Colorectal Cancer Atlas

Single-cell integration and multi-modal profiling reveals phenotypes and spatial organization of neutrophils in colorectal cancer

The single cell colorectal cancer atlas is a resource integrating more than 4.27 million cells from 650 patients across 49 studies (77 datasets) representing 7 billion expression values. These samples encompass the full spectrum of disease progression, from normal colon to polyps, primary tumors, and metastases, covering both early and advanced stages of CRC. Additionally, to address the limited availability of neutrophil single-cell data, we supplemented the atlas by analyzing samples from 12 CRC patients using a platform that captures cells with very low transcript counts. We present a high-resolution view of CRC with 62 major cell types or states, revealing different cell-type composition patterns in CRC subtypes.

Atlas overview UMAP

Browse or get the full CRC atlas

Browse and interactively explore the full atlas on our local cellxgene instance.

If you are interested in running your own analyses on the full atlas, you can download the h5ad file with standardized metadata.

CZI cell-x-gene portal

The core-atlas will become available on the CZI cell-x-gene soon. There, you will be able to explore the datasets interactively in the browser and download them as h5ad (scverse) or rds (Seurat) files with standardized metadata for further analysis.

Browse code

All code needed to reproduce the study is wrapped into a nextflow workflow and publicy available from GitHub.

Download additional data

In addition to the h5ad objects mentioned above, we provide preprocessed input data, intermediate results and final results on zenodo.

Spatial transcriptomics (Xenium) and Imaging Mass Cytometry (IMC) data may be downloaded from BioImage Archive.

Contact

For reproducibility issues or any other requests regarding single-cell data analysis, please use the issue tracker. For anything else, you can reach out to the corresponding author(s) as indicated in the manuscript.