ChIPseqSpikeInFree: a ChIP-seq normalization approach to reveal global changes in histone modifications without spike-in
Open accessAbstract
Motivation: The traditional reads per million normalization method is inappropriate for the evaluation of ChIP-seq data when treatments or mutations have global effects. Changes in global levels of histone modifications can be detected with exogenous reference spike-in controls. However, most ChIP-seq studies overlook the normalization that must be corrected with spike-in. A method that retrospectively renormalizes datasets without spike-in is lacking. Results: ChIPseqSpikeInFree is a novel ChIP-seq normalization method to effectively determine scaling factors for samples across various conditions and treatments, which does not rely on exogenous spike-in chromatin or peak detection to reveal global changes in histone modification occupancy. Application of ChIPseqSpikeInFree on five datasets demonstrates that this in silico approach reveals a similar magnitude of global changes as the spike-in method does. Availability and implementation: St. Jude Cloud (https://pecan.stjude.cloud/permalink/spikefree) and St. Jude Github ( https://github.com/stjude/ChIPseqSpikeInFree). Supplementary information: Supplementary data are available at Bioinformatics online.
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For the histone mark H3K14ac, the recommended histone ChIP-seq normalization pipeline was used to generate scale factors.
“For the histone mark H3K14ac, we used the recommended histone ChIP-seq normalization pipeline64 to generate scale factors.”
From HBO1 functions as an epigenetic barrier to hepatocyte plasticity and reprogramming during liver injury (2025) · cites this paper as [64]
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References 22 · Cited by 57
- Authors
- Jin, H., Kasper, L. H., Larson, J. D., Wu, G., Baker, S. J., Zhang, J., & Fan, Y.
- Affiliations
- St. Jude Children's Research Hospital (US)
- Corresponding author
- Fan, Yiping
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2019-09-30
- Volume
- 36
- Issue
- 4
- Pages
- 1270-1272
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- OpenAlex
- W2979008768
- Cited by
- 57
- References
- 22
- Citations by year
- 2026: 8 · 2025: 7 · 2024: 10 · 2023: 16 · 2022: 6 · 2021: 8 · 2020: 2
- FWCI
- 1.32
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Bioinformatics (publishedVersion, public-domain)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (P30CA021765)
- National Institutes of Health (P01CA096832)
- American Lebanese Syrian Associated Charities
- 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
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- spike-in controls, histone modifications, scale factor
- MeSH terms
- Chromatin Immunoprecipitation Sequencing, Chromatin, Retrospective Studies, Sequence Analysis, DNA, Histone Code, Chromatin Immunoprecipitation
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