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map3C: a computational tool for processing multiomic single-cell Hi-C data
Joseph Galasso1,2,3, Ye Wang1,4,5,6, Frank Alber4,6
1Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles CA 90095, USA.
Biorxiv : the Preprint Server for Biology
|November 25, 2025
Summary
New software, map3C, enhances multiomic single-cell Hi-C data analysis. This tool improves data quality and aids in identifying genomic structural variant locations.
Area of Science:
- Genomics
- Epigenetics
- Bioinformatics
Background:
- Multiomic single-cell Hi-C methods offer novel insights into genome structure-function relationships by profiling chromatin conformation alongside other molecular data.
- Current bioinformatics tools face limitations in processing these complex multiomic datasets, hindering downstream analysis.
Purpose of the Study:
- To introduce map3C, a novel software tool designed to overcome existing limitations in multiomic single-cell Hi-C data analysis.
- To demonstrate the effectiveness of map3C in improving data quality and enabling the identification of structural variants.
Main Methods:
- Development of map3C software for processing multiomic single-cell Hi-C data.
- Evaluation of map3C's performance in enhancing data quality for downstream bioinformatics analyses.
- Application of map3C to identify genomic structural variant locations.
Main Results:
- map3C significantly improves the quality of multiomic single-cell Hi-C data.
- The software facilitates more robust downstream bioinformatics analysis.
- map3C demonstrates utility in pinpointing locations of structural variants within the genome.
Conclusions:
- map3C addresses critical limitations in current multiomic single-cell Hi-C data processing.
- The tool enhances the analytical capabilities for studying genome structure and function.
- map3C is a valuable resource for researchers investigating genomic structural variations.

