EpiCypher’s CUTANA™ Fiber-seq Services provide biotech and academic researchers with unique access to our genomic expertise and multiomic capabilities, enabling diverse applications across biomedical research and drug development.

Taking advantage of EpiCypher’s Fiber-seq services gives you expert access to single-molecule, multiomic profiling of chromatin accessibility, DNA methylation, and DNA sequence.

By integrating these layers of information using long-read sequencing, Fiber-seq delivers insights far beyond what is possible with conventional approaches like ATAC-seq or bisulfite sequencing.

As our partner, you can expect to:

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Fiber-seq is a novel LRS-based multiomic mapping assay that leverages DNA methyltransferase (MTase) Hia5 to label open chromatin with N6-methyladenosine (6mA). Unlike existing assays that require chromatin fragmentation, this approach preserves the DNA molecules intact for LRS. 

Fiber-seq is the first commercially available chromatin accessibility assay that leverages long-read sequencing. In Fiber‑seq, nuclei are isolated and then incubated with Hia5 6mA MTase. The cofactor for Hia5, S‑adenosylmethionine (SAM), is added, which activates the Hia5 to induce methylation of adenines within accessible chromatin in as short as 10 minutes. Following, the enzyme is quenched, high molecular weight (HMW) DNA is purified, and the sample is prepared for LRS following standard protocols. 

The portion of the Fiber-seq protocol before sequencing is quick and easy, comparable to the time it takes to perform ATAC-seq – or even faster.

Our Services team is highly skilled at performing the Fiber-seq assay and data analysis, and is ready to help you get started with your experiment!

Why Consider CUTANA™ Fiber-seq Services?

Leverage EpiCypher’s Fiber-seq services to achieve:

  • Multiomic insights in one assay – Fiber-seq simultaneously profiles chromatin accessibility, DNA methylation, and genetic variants, consolidating what typically requires three or more separate assays into one long-read sequencing assay.

  • Highest activity 6mA-MTase – Faster labeling via Hia5 enables higher resolution of accessible DNA, with demonstrated utility in protein footprinting applications to resolve transcription factor binding and nucleosome positioning [2-4].

  • Access complex genomic regions – Profile chromatin accessibility in repetitive and structurally complex regions such as transposable elements, centromeres, telomeres, segmental duplications, and chromosomal rearrangements.

  • Resolve chromatin state heterogeneity – PCR-free approach leverages long-read sequencing to directly profile individual DNA molecules, uncovering heterogeneity of complex cell populations often missed by short-read techniques.

For detailed technical information about the Fiber-seq assay please see the Fiber-seq protocol

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