Cooler: scalable storage for Hi-C data and other genomically labeled arrays
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Abstract
Motivation: Most existing coverage-based (epi)genomic datasets are one-dimensional, but newer technologies probing interactions (physical, genetic, etc.) produce quantitative maps with two-dimensional genomic coordinate systems. Storage and computational costs mount sharply with data resolution when such maps are stored in dense form. Hence, there is a pressing need to develop data storage strategies that handle the full range of useful resolutions in multidimensional genomic datasets by taking advantage of their sparse nature, while supporting efficient compression and providing fast random access to facilitate development of scalable algorithms for data analysis. Results: We developed a file format called cooler, based on a sparse data model, that can support genomically labeled matrices at any resolution. It has the flexibility to accommodate various descriptions of the data axes (genomic coordinates, tracks and bin annotations), resolutions, data density patterns and metadata. Cooler is based on HDF5 and is supported by a Python library and command line suite to create, read, inspect and manipulate cooler data collections. The format has been adopted as a standard by the NIH 4D Nucleome Consortium. Availability and implementation: Cooler is cross-platform, BSD-licensed and can be installed from the Python package index or the bioconda repository. The source code is maintained on Github at https://github.com/mirnylab/cooler. Supplementary information: Supplementary data are available at Bioinformatics online.
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Hi-C data was mapped to mm10 and converted to .cool format considering only read pairs with both sides mapping with high confidence (mapq ≥30).
“Data was mapped to mm10 using the distiller-nf pipeline (https://github.com/open2c/distiller-nf), iteratively corrected and converted into .cool format with cooler (85), only considering read pairs with both sides mapping with high confidence (mapq ≥30).”
From Synergy between regulatory elements can render cohesin dispensable for distal enhancer function (2026) · cites this paper as [85]
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- Authors
- Abdennur, N., & Mirny, L. A.
- Affiliations
- Institute for Medical Engineering and Science, Cambridge, MA 02139, USA
- Massachusetts Institute of Technology (US)
- Corresponding author
- Abdennur, Nezar
- Mirny, Leonid A
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2019-07-10
- Volume
- 36
- Issue
- 1
- Pages
- 311-316
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- PMC
- PMC8205516
- OpenAlex
- W2960979937
- Cited by
- 1,759
- References
- 3
- Citations by year
- 2026: 158 · 2025: 382 · 2024: 638 · 2023: 375 · 2022: 100 · 2021: 58 · 2020: 35 · 2019: 13
- FWCI
- 17.78
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- Locations
- Bioinformatics (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health Common Fund 4D Nucleome Program
- Center for Structure and Physics of the Genome (DK107980)
- 4D Nucleome Network Data Coordination and Integration Center (U01 CA200059)
- NIH
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Social Sciences › Decision Sciences › Information Systems and Management › Scientific Computing and Data Management
- Keywords
- Hi-C data, HDF5, data compression, scalable data storage, Python library
- MeSH terms
- Metadata, Algorithms, Software, Information Storage and Retrieval, Genomics
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