TY - JOUR
T1 - The Curated Cancer Cell Atlas provides a comprehensive characterization of tumors at single-cell resolution
AU - Tyler, Michael
AU - Gavish, Avishai
AU - Barbolin, Chaya
AU - Tschernichovsky, Roi
AU - Hoefflin, Rouven
AU - Mints, Michael
AU - Puram, Sidharth V.
AU - Tirosh, Itay
N1 - Publisher Copyright: © The Author(s), under exclusive licence to Springer Nature America, Inc. 2025.
PY - 2025/5/8
Y1 - 2025/5/8
N2 - Recent years have seen a rapid proliferation of single-cell cancer studies, yet most of these studies profiled few tumors, limiting their statistical power. Combining data and results across studies holds great promise but also involves various challenges. We recently began to address these challenges by curating a large collection of cancer single-cell RNA-sequencing datasets, leveraging it for systematic analyses of tumor heterogeneity. Here we greatly extend this repository to 124 datasets for over 40 cancer types, together comprising 2,836 samples, with improved data annotations, visualizations and exploration. Using this vast cohort, we generate an updated map of recurrent expression programs in malignant cells and systematically quantify context-dependent gene expression and cell-cycle patterns across cell types and cancer types. These data, annotations and analysis results are all freely available for exploration and download through the Curated Cancer Cell Atlas, a central community resource that opens new avenues in cancer research.
AB - Recent years have seen a rapid proliferation of single-cell cancer studies, yet most of these studies profiled few tumors, limiting their statistical power. Combining data and results across studies holds great promise but also involves various challenges. We recently began to address these challenges by curating a large collection of cancer single-cell RNA-sequencing datasets, leveraging it for systematic analyses of tumor heterogeneity. Here we greatly extend this repository to 124 datasets for over 40 cancer types, together comprising 2,836 samples, with improved data annotations, visualizations and exploration. Using this vast cohort, we generate an updated map of recurrent expression programs in malignant cells and systematically quantify context-dependent gene expression and cell-cycle patterns across cell types and cancer types. These data, annotations and analysis results are all freely available for exploration and download through the Curated Cancer Cell Atlas, a central community resource that opens new avenues in cancer research.
UR - http://www.scopus.com/inward/record.url?scp=105004709072&partnerID=8YFLogxK
U2 - 10.1038/s43018-025-00957-8
DO - 10.1038/s43018-025-00957-8
M3 - مقالة
SN - 1474-175X
JO - Nature Cancer
JF - Nature Cancer
M1 - 4076
ER -