Transform Your Long-Read Sequencing Into a Multiomic Powerhouse
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CUTANA™ Hia5 is the essential enzyme for Fiber-seq [1], a cutting-edge multiomic long-read sequencing (LRS) assay that simultaneously profiles chromatin accessibility, DNA methylation, and genetic variation at single-molecule resolution. By layering chromatin accessibility on top of standard LRS workflows, Fiber-seq uniquely links epigenetic information (DNA methylation) and complex genetic architecture, including structural variants and haplotype phasing, to chromatin states within the same DNA molecules (Figure 1). |
15% off with code FSEQ15 until December 31, 2026
Offer non-cumulative with any other discounts, special offers or price agreements.

Figure 1: Overview of the CUTANA Fiber-Seq protocol.
How Fiber-seq Works
CUTANA™ Hia5 is a DNA adenine methyltransferase (MTase) that uses S-adenosylmethionine (SAM) to catalyse methylation at the N6 position of adenine, producing N6-methyladenine (6mA).
In Fiber-seq, Hia5’s nonspecific activity methylates adenines within accessible chromatin regions in situ, effectively recording chromatin accessibility onto native DNA without disturbing endogenous methylation (5mC).
The Hia5-modified DNA is fully compatible with long-read sequencing platforms, including PacBio® HiFi Sequencing and ONT® Nanopore Sequencing, ensuring seamless integration into your existing workflows.

Figure 2: Fiber-seq simultaneously detects open chromatin (6mA) and DNA methylation (5mC).
Why CUTANA™ Hia5 Is a Game-Changer
- Multiomic insights in a single assay
Consolidate multiple assays into one: Fiber-seq simultaneously profiles chromatin accessibility, DNA methylation, and genetic variants, reducing cost, time, and sample requirements. - Highest-activity 6mA-MTase
Hia5 enables faster labelling and higher-resolution mapping of accessible DNA, with proven applications in protein footprinting, including transcription factor binding and nucleosome positioning [2–4] (refer to Figure 2). - Access the hardest-to-sequence regions
Profile chromatin accessibility in repetitive and structurally complex regions such as transposable elements, centromeres, telomeres, segmental duplications, and chromosomal rearrangements. - Easy workflow integration
Perform Fiber-seq in less than 2 hours, directly upstream of standard long-read sequencing library preparation (illustrated in Figure 1). - Resolve chromatin state heterogeneity
Our PCR-free approach leverages long-read sequencing to profile individual DNA molecules, uncovering heterogeneity in cell populations often missed by short-read methods.
CUTANA™ Hia5: Product Specifications
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Ready to elevate your chromatin and epigenomic research? Fill out the form below to contact us to learn more about CUTANA™ Hia5 and Fiber-seq, and discover how our multiomic solutions can empower your experiments.
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References
Article content created by Tebubio using courtesy materials provided by EpiCypher.
Source 1: Stergachis AB, Debo BM, Haugen E, Churchman LS, Stamatoyannopoulos JA. "Single-molecule regulatory architectures captured by chromatin fiber sequencing" Science. 2020;368(6498):1449-1454. doi:10.1126/science.aaz1646.
Source 2: Tullius TW, Isaac RS, Dubocanin D, Ranchalis J, Churchman LS, Stergachis AB. "RNA polymerases reshape chromatin architecture and couple transcription on individual fibers" Mol Cell. 2024;84(17):3209-3222.e5. doi:10.1016/j.molcel.2024.08.013.
Source 3: Dubocanin D, Hartley GA, Sedeño Cortés AE, et al. "Conservation of dichromatin organization along regional centromeres" Cell Genom. 2025;5(4):100819. doi:10.1016/j.xgen.2025.100819.
Source 4: Vollger MR, Swanson EG, Neph SJ, et al. "A haplotype-resolved view of human gene regulation" Preprint. bioRxiv. 2025;2024.06.14.599122. Published 2025 Jun 2. doi:10.1101/2024.06.14.599122.
Source 5: Jha A, Bohaczuk SC, Mao Y, et al. "DNA-m6A calling and integrated long-read epigenetic and genetic analysis with fibertools" Genome Res. 2024;34(11):1976-1986. Published 2024 Nov 20. doi:10.1101/gr.279095.124.
