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Updated: Jun 15, 2026

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations
Published on: April 21, 2023
Unified molecular approach for spatial epigenome, transcriptome, and cell lineages
Yung-Hsin Huang1, Julia A Belk1, Ruochi Zhang2,3,4
1Department of Dermatology, Center for Personal Dynamic Regulomes and Program in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305.
SPACE-seq enables spatial multiomics using standard reagents, overcoming limitations of bespoke methods. This new technique reveals tumor microenvironment states and genetic variations in glioblastoma.
Area of Science:
- Genomics
- Epigenomics
- Molecular Biology
Background:
- Spatial epigenomics and multiomics offer detailed cellular insights.
- Current methods require specialized slides and chemistries, limiting accessibility.
- A unified approach for spatial multiomics is needed.
Purpose of the Study:
- Introduce SPACE-seq, a novel method for spatial multiomics.
- Enable facile spatial multiomics using standard reagents.
- Characterize glioblastoma using spatial multiomics.
Main Methods:
- Developed SPACE-seq utilizing polyadenine-tailed epigenomic libraries.
- Employed standard whole transcriptome reagents for library preparation.
- Applied SPACE-seq to a human glioblastoma specimen.
Main Results:
- Revealed the cellular states within the glioblastoma tumor microenvironment.
- Determined extrachromosomal DNA copy numbers spatially.
- Identified putative mitochondrial DNA variants within the specimen.
Conclusions:
- SPACE-seq facilitates spatial multiomics with existing reagents.
- The method provides comprehensive insights into complex biological samples.
- SPACE-seq is a powerful tool for studying diseases like glioblastoma.
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