CZ CELLxGENE Discover: a single-cell data platform for scalable exploration, analysis and modeling of aggregated data
Open accessAbstract
Hundreds of millions of single cells have been analyzed using high-throughput transcriptomic methods. The cumulative knowledge within these datasets provides an exciting opportunity for unlocking insights into health and disease at the level of single cells. Meta-analyses that span diverse datasets building on recent advances in large language models and other machine-learning approaches pose exciting new directions to model and extract insight from single-cell data. Despite the promise of these and emerging analytical tools for analyzing large amounts of data, the sheer number of datasets, data models and accessibility remains a challenge. Here, we present CZ CELLxGENE Discover (cellxgene.cziscience.com), a data platform that provides curated and interoperable single-cell data. Available via a free-to-use online data portal, CZ CELLxGENE hosts a growing corpus of community-contributed data of over 93 million unique cells. Curated, standardized and associated with consistent cell-level metadata, this collection of single-cell transcriptomic data is the largest of its kind and growing rapidly via community contributions. A suite of tools and features enables accessibility and reusability of the data via both computational and visual interfaces to allow researchers to explore individual datasets, perform cross-corpus analysis, and run meta-analyses of tens of millions of cells across studies and tissues at the resolution of single cells.
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The exponential increase in throughput of measurement technologies has led to collection of large and growing reference datasets within and across different cell and tissue systems, with data doubling every 6 months for the past several years.
“Experimentally, the exponential increase in the throughput of measurement technologies has led to the collection of large and growing reference datasets within and across different cell and tissue systems,23–25 with data doubling every 6 months for the past several years,26”
From How to build the virtual cell with artificial intelligence: Priorities and opportunities (2024) · cites this paper as [25]
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- Authors
- Program, C. C. S., Abdulla, S., Aevermann, B., Assis, P., Badajoz, S., Bell, S. M., Bezzi, E., Cakir, B., Chaffer, J., Chambers, S., Cherry, J. M., Chi, T., Chien, J., Dorman, L., Garcia-Nieto, P., Gloria, N., Hastie, M., Hegeman, D., Hilton, J., Huang, T., Infeld, A., Istrate, A.-M., Jelic, I., Katsuya, K., Kim, Y. J., Liang, K., Lin, M., Lombardo, M., Marshall, B., Martin, B., McDade, F., Megill, C., Patel, N., Predeus, A., Raymor, B., Robatmili, B., Rogers, D., Rutherford, E., Sadgat, D., Shin, A., Small, C., Smith, T., Sridharan, P., Tarashansky, A., Tavares, N., Thomas, H., Tolopko, A., Urisko, M., Yan, J., Yeretssian, G., Zamanian, J., Mani, A., Cool, J., & Carr, A.
- Affiliations
- Wellcome Sanger Institute (GB)
- Chan Zuckerberg Initiative (United States) (US)
- Wellcome Sanger Institute, Wellcome Genome Campus , Hinxton CB10 1SA ,
- Chan Zuckerberg Biohub San Francisco (US)
- Chan Zuckerberg Initiative , 1180 Main Street, Redwood City, CA 94063 ,
- Stanford Medicine (US)
- Corresponding author
- Mani, Arathi
- Cool, Jonah
- Carr, Ambrose
- ORCID
- Abdulla, Shibla
- Aevermann, Brian
- Assis, Pedro
- Bell, Sidney M
- Bezzi, Emanuele
- Cherry, J Michael
- Chien, Jennifer
- Dorman, Leah
- Hilton, Jason
- Istrate, Ana-Maria
- Kim, Yang Joon
- Marshall, Bailey
- Predeus, Alexander
- Rutherford, Erica
- Small, Corinn
- Tarashansky, Alexander
- Tavares, Norbert
- Yeretssian, Garabet
- Zamanian, Jennifer
- Cool, Jonah
- Carr, Ambrose
- Venue
- Nucleic Acids Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2024-11-28
- Volume
- 53
- Issue
- D1
- Pages
- D886-D900
- ISSN
- 0305-1048 (ISSN-L)
- 1362-4962
- PMC
- PMC11701654
- OpenAlex
- W4404793799
- Cited by
- 399
- References
- 14
- Citations by year
- 2026: 219 · 2025: 163 · 2024: 16 · 2023: 1
- FWCI
- 54.18
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Nucleic Acids Research (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Social Sciences › Decision Sciences › Information Systems and Management › Scientific Computing and Data Management
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Keywords
- single-cell transcriptomics, meta-analysis, large language models, data reusability
- MeSH terms
- Machine Learning, Humans, Software, Computational Biology, Gene Expression Profiling, Single-Cell Analysis, Transcriptome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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