Provide AI-ready datasets and provenance for mapping human cell architecture from disease-relevant cell lines, enabling machine learning and AI research on genomics, proteomics, and imaging modalities.
Grantor
Grant Name
Grant Number
National Institutes of Health
Bridge2AI program
1OT2OD032742-01
📊
Composition
What do the instances represent?
Counts
Data Type
Instance Type
Label
Name
Representation
11739
Raw sequencing reads and processed gene-expression/fitness features (per RO-Crate packages).
Single cells; gene perturbations
Transcriptional and fitness phenotypes per targeted gene perturbation.
CRISPRi perturb-seq in KOLF2.1J hiPSCs
Single-cell transcriptomes and fitness phenotypes from CRISPRi perturbations in undifferentiated KOL...
563
Multi-channel immunofluorescence images under untreated and drug-treated conditions (vorinostat, pac...
Cell images; protein localization
Protein-of-interest localization patterns across conditions.
Protein localization IF imaging in MDA-MB-468
Immunofluorescence confocal microscopy images with four channels (DAPI, ER/calreticulin, tubulin, pr...
Mass spectrometry intensity profiles indicative of protein complex size distributions.
Proteins; chromatographic fractions
Protein-protein interaction SEC-MS
Size exclusion chromatography–mass spectrometry profiles from undifferentiated KOLF2.1J iPSCs and iP...
Identification
Undifferentiated KOLF2.1J human iPSCs and iPSC-derived NPCs, neurons, and cardiomyocytes.
MDA-MB-468 breast cancer cells (untreated and treated with vorinostat or paclitaxel).
Distribution
Multiple experimental conditions including presence/absence of chemotherapy.
Cell Maps for Artificial Intelligence - March 2025 Data Release (Beta)
Cell Maps for Artificial Intelligence - March 2025 Data Release (Beta)
This dataset is the March 2025 Data Release of Cell Maps for Artificial Intelligence (CM4AI; CM4AI.org), the Functional Genomics Grand Challenge in the NIH Bridge2AI program. This Beta release includes perturb-seq data in undifferentiated KOLF2.1J iPSCs; SEC-MS data in undifferentiated KOLF2.1J iPSCs and iPSC-derived NPCs, neurons, and cardiomyocytes; and IF images in MDA-MB-468 breast cancer cells in the presence and absence of chemotherapy (vorinostat and paclitaxel). CM4AI output data are packaged with provenance graphs and rich metadata as AI-ready datasets in RO-Crate format using the FAIRSCAPE framework. Data presented here will be augmented regularly through the end of the project. CM4AI is a collaboration of UCSD, UCSF, Stanford, UVA, Yale, UA Birmingham, Simon Fraser University, and the Hastings Center. This data is Copyright (c) 2025 The Regents of the University of California except where otherwise noted. Spatial proteomics raw image data is copyright (c) 2025 The Board of Trustees of the Leland Stanford Junior University. Dataset licensed for reuse under Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International license (https://creativecommons.org/licenses/by-nc-sa/4.0/). Attribution is required to the copyright holders and the authors. Any publications referencing this data or derived products should cite the Related Publication below, as well as directly citing this data collection (2025-03-04). (2025-03-07)
Create standardized, provenance-rich, FAIR AI-ready datasets to accelerate AI methods for functional genomics and cell architecture mapping.
Role
Name
ORCID
Affiliation
Principal Investigator
Trey Ideker
-
Cell Maps for Artificial Intelligence (CM4AI)
Principal Investigator
Emma Lundberg
-
Stanford University
Principal Investigator
Nevan Krogan
-
University of California San Francisco
Description
Data acquired via high-throughput scRNAseq (perturb-seq), confocal fluorescence microscopy (IF), and SEC-MS proteomics.
Was Directly Observed
True
Was Reported By Subjects
False
Was Inferred Derived
partial
Was Validated Verified
not specified
Description
Hardware and instruments include sequencing platforms for scRNAseq, confocal microscopes for IF imaging, and mass spectrometers for SEC-MS; datasets packaged as RO-Crates using the FAIRSCAPE framework.
Description
Lundberg Lab at Stanford University (IF imaging).
Nevan Krogan Laboratory at UCSF (SEC-MS).
CM4AI collaboration across UCSD, UCSF, Stanford, UVA, Yale, UAB, Simon Fraser University, and the Hastings Center.
Description
Data creation date 2025-02-27; published 2025-03-03.
External Resources
SEC-MS data will be uploaded to PRIDE when available.
Future Guarantees
Not specified.
Archival
Planned archival in PRIDE for proteomics data.
Restrictions
Subject to repository terms and the dataset’s CC BY-NC-SA 4.0 license.
Description
No individually identifiable human data; experiments are on established human cell lines.
Description
Point Of Contact
Trey Ideker (University of California San Diego). Contact via Dataverse dataset page.
Compression
Description
Format
Is Tabular
Issued
Md5
Media Type
Name
Title
RO-Crate metadata for the expressed genome-scale CRISPRi Perturbation Cell Atlas in undifferentiated...
Analysis and model development using CRISPRi perturb-seq scRNAseq, SEC-MS protein interaction profiling, and immunofluorescence protein localization images.
Description
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). Attribution required to the copyright holders and the authors.
Description
Related publications include bioRxiv preprints on CM4AI cell maps and the perturbation cell atlas (e.g., doi:10.1101/2024.05.21.589311; doi:10.1101/2024.11.03.621734).