Abstract
AbstractSummaryGene regulation is intricately influenced by the three-dimensional organization of the genome. In particular, chromatin can exist in loop structures that enable long-range regulatory interactions. By utilizing chromosome conformation capture techniques such as Hi-C, valuable information regarding the organization of these loop structures in 3D space can be obtained. While functional/feature enrichment has become a standard downstream analysis for different genomic data to provide biological context, tools that developed specifically for high throughput assays capturing chromosome conformation are relatively limited. Here, we present Loopsim, a command-line application that performs enrichment analysis on Hi-C loop profiles against user-defined regions. Loopsim efficiently simulates a background distribution using a distinctive sampling approach that considers loop size, intervals, loop-loop distances, and structure; it then computes loop-level statistics based on the empirical null distribution.AvailabilityLoopsim is a Python package available via PyPI (https://pypi.org/project/loopsim) and the source code is available on GitHub (https://github.com/CutaneousBioinf/Loopsim) under the MIT license.
Publisher
Cold Spring Harbor Laboratory
Reference17 articles.
1. Berkum, N.L.v. , et al. Hi-C: A Method to Study the Three-dimensional Architecture of Genomes. JoVE (Journal of Visualized Experiments) 2010(39):e1869.
2. Accurate loop calling for 3D genomic data with cLoops
3. An integrated model for detecting significant chromatin interactions from high-resolution Hi-C data;Nature Communications,2017
4. Dand, N. , et al. GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets. In.: medRxiv; 2023.
5. Juicer Provides a One-Click System for Analyzing Loop-Resolution Hi-C Experiments