Evidence map›Paper›PMID 42730630›Full record

ArticleBioinformatics (Oxford, England)2026

dcHiChIP: a comprehensive Nextflow-based pipeline for multiscale analysis of chromatin architecture from HiChIP data.

Abhishek Agarwal, Ziad Al Bkhetan, Dariusz Plewczynski

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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Abhishek AgarwalUniversity of Warsaw, Centre of New Technologies, Laboratory of Functional and Structural Genomics, Banacha 2c, Warsaw, Mazovia, 02-097, Poland.ORCID 0000-0003-4981-8746
Ziad Al BkhetanAustralian BioCommons, The University of Melbourne, North Melbourne, VIC 3051, Australia.ORCID 0000-0002-4032-5331
Dariusz PlewczynskiUniversity of Warsaw, Centre of New Technologies, Laboratory of Functional and Structural Genomics, Banacha 2c, Warsaw, Mazovia, 02-097, Poland.ORCID 0000-0002-3840-7610

Funding

Nucleome Positioning System for Spatiotemporal Genome Organization and RegulationU54DK107967 · NIDDK · JACKSON LABORATORY · PI WEI, CHIA-LIN · 2015 to 2019
$3.6M
Laboratory of Bioinformatics and Computational Genomics, Faculty of Mathematics and Information Science, Warsaw University of TechnologyNIDDK NIH HHS U54 DK107967NIH HHSPolish Ministry of Science and Higher Education 7054/IA/SP/2020Polish National Science Centre 2020/37/B/NZ2/03757USA 4DNucleome 1U54DK107967-01Warsaw University of Technology within the Excellence Initiative: Research University (IDUB)
6 · The paper itself

Abstract

motivationDespite the growing use of HiChIP to investigate protein-directed chromatin architecture, a comprehensive and reproducible pipeline for analysing these datasets-from raw reads to multiscale 3D genome features-remains lacking. Existing tools often focus on isolated components, such as loop calling or matrix generation, but fall short in integrating structural annotation, functional enrichment, and spatial modeling within a unified framework. To address this gap, we developed dcHiChIP, a modular, scalable Nextflow-based workflow that streamlines the analysis of HiChIP data, enabling both routine processing and in-depth exploration of chromatin organization and regulatory interactions.

resultsdcHiChIP enables robust and reproducible analysis of HiChIP datasets across multiple scales of chromatin architecture. It accepts raw sequencing data as input and generates high-quality loop calls, domain annotations, and 3D genome models. It also performs functional annotation and motif enrichment analyses. Applied to benchmark CTCF HiChIP datasets, dcHiChIP identifies major chromatin architectural features such as TADs/CCDs, A/B compartments, and chromatin stripes, and offers efficient, end-to-end execution with support for batch processing and workflow resumability. AVAILABILITY: dcHiChIP is publicly available on GitHub at https://github.com/SFGLab/dcHiChIP, with documentation at https://sfglab.github.io/dcHiChIP/. The software version used in this study is archived at Zenodo: https://doi.org/10.5281/zenodo.22030542.

Indexed as

ChromatinComputational BiologyHigh-Throughput Nucleotide SequencingSoftwareChromatin

Identifiers

PMID42730630
PMCPMC13576066

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.