Evidence map›Paper›PMID 30064362›Full record

ArticleBMC bioinformatics2018

HiCcompare: an R-package for joint normalization and comparison of HI-C datasets.

John C Stansfield, Kellen G Cresswell, Vladimir I Vladimirov, Mikhail G Dozmorov

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

85 citing papers in PubMed.

  1. Article
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  4. PDS5A and TOP2B cooperate for chromatin recruitment via CTCF.bioRxiv : the preprint server for biology · 2026
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  7. Differential analysis of image-based chromatin tracing data with Dory.bioRxiv : the preprint server for biology · 2026
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  19. Review
  20. Read Mapping for Hi-C Analysis.Methods in molecular biology (Clifton, N.J.) · 2025
    Article

25 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

John C StansfieldDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA, 23298, USA.
Kellen G CresswellDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA, 23298, USA.
Vladimir I VladimirovDepartment of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Richmond, VA, 23219, USA.
Mikhail G DozmorovDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA, 23298, USA. mikhail.dozmorov@vcuhealth.org.ORCID 0000-0002-0086-8358

Funding

Integration of Mixtures Toxicology, Toxicogenomics, and StatisticsT32ES007334 · NIEHS · VIRGINIA COMMONWEALTH UNIVERSITY · PI WHEELER, DAVID CHARLES · 2002 to 2018
$2.5M
American Cancer Society IRG-14-192-40NIEHS NIH HHS T32 ES007334NIEHS NIH HHS T32ES007334
6 · The paper itself

Abstract

backgroundChanges in spatial chromatin interactions are now emerging as a unifying mechanism orchestrating the regulation of gene expression. Hi-C sequencing technology allows insight into chromatin interactions on a genome-wide scale. However, Hi-C data contains many DNA sequence- and technology-driven biases. These biases prevent effective comparison of chromatin interactions aimed at identifying genomic regions differentially interacting between, e.g., disease-normal states or different cell types. Several methods have been developed for normalizing individual Hi-C datasets. However, they fail to account for biases between two or more Hi-C datasets, hindering comparative analysis of chromatin interactions.

resultsWe developed a simple and effective method, HiCcompare, for the joint normalization and differential analysis of multiple Hi-C datasets. The method introduces a distance-centric analysis and visualization of the differences between two Hi-C datasets on a single plot that allows for a data-driven normalization of biases using locally weighted linear regression (loess). HiCcompare outperforms methods for normalizing individual Hi-C datasets and methods for differential analysis (diffHiC, FIND) in detecting a priori known chromatin interaction differences while preserving the detection of genomic structures, such as A/B compartments.

conclusionsHiCcompare is able to remove between-dataset bias present in Hi-C matrices. It also provides a user-friendly tool to allow the scientific community to perform direct comparisons between the growing number of pre-processed Hi-C datasets available at online repositories. HiCcompare is freely available as a Bioconductor R package https://bioconductor.org/packages/HiCcompare/ .

Indexed as

Databases, GeneticSoftwareAnimalsCCCTC-Binding FactorCell DifferentiationChromatinComputational BiologyGenomeHumansMiceNeuronsCCCTC-Binding FactorChromatinChromosome conformation captureComparisonDifferential analysisHi-CHiCcompareNormalization

Identifiers

PMID30064362
PMCPMC6069782

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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.