Guiding the design of well-powered Hi-C experiments to detect differential loops
Abstract
3D chromatin structure plays an important role in gene regulation by connecting regulatory regions and gene promoters. The ability to detect the formation and loss of these loops in various cell types and conditions provides valuable information on the mechanisms driving these cell states and is critical for understanding how long-range gene regulation works. Hi-C is a powerful technique used to characterize three-dimensional chromatin structure; however, Hi-C can quickly become a costly and labor-intensive endeavor, and proper planning is required to determine how to best use time and resources while maintaining experimental rigor and well-powered results. To facilitate better planning and interpretation of Hi-C experiments, we have conducted a detailed evaluation of statistical power using publicly available Hi-C datasets paying particular attention to the impact of loop size on Hi-C contacts and fold change compression. In addition, we have developed Hi-C Poweraid, a publicly-hosted web application to investigate these findings (http://phanstiel-lab.med.unc.edu/poweraid/). For experiments involving well-replicated cell lines, we recommend a total sequencing depth of at least 6 billion contacts per condition, split between at least 2 replicates in order to achieve the power to detect the majority of differential loops. For experiments with higher variation, more replicates and deeper sequencing depths are required. Exact values and recommendations for specific cases can be determined through the use of Hi-C Poweraid. This tool simplifies the complexities behind calculating power for Hi-C data and will provide useful information on the amount of well-powered loops an experiment will be able to detect given a specific set of experimental parameters, such as sequencing depth, replicates, and the sizes of the loops of interest. This will allow for more efficient use of time and resources and more accurate interpretation of experimental results. HIGHLIGHTSO_LIDistance-dependent Hi-C contacts and fold change compression influence power C_LIO_LIIntegrative modeling of Hi-C power provides guidance for experimental design C_LIO_LIAn interactive web app aids the design of differential Hi-C experiments C_LI
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 5
- FWCI
- 0.44
- Field percentile
- top 47%
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Systematic assessment of sequencing depth requirements for Hi-C-derived metrics
Alexander Granovsky, Kirill Polovnikov·bioRxiv·Aug 1, 2026
- DeepHiC: A Generative Adversarial Network for Enhancing Hi-C Data Resolution
Hao Hong, Shuai Jiang, … Xiaochen Bo·PLoS Computational BiologyPeer-reviewed·Feb 21, 2020
- ChiCMaxima: a robust and simple pipeline for detection and visualization of chromatin looping in Capture Hi-C
Yousra Ben Zouari, Anne Marie Molitor, … Tom Sexton·Genome biologyPeer-reviewed·May 22, 2019
- DiffHiChIP: Identifying differential chromatin contacts from HiChIP data
Sourya Bhattacharyya, Daniela Salgado Figueroa, … Ferhat Ay·Cell Reports MethodsPeer-reviewed·Nov 1, 2025
- Extracting multi-way chromatin contacts from Hi-C data
- Enhancing Hi-C contact matrices for loop detection with Capricorn, a multi-view diffusion model
Tangqi Fang, Yifeng Liu, … Sheng Wang·BioinformaticsPeer-reviewed·Jun 28, 2024