Diagenode

Assay for Transposase-Accessible Chromatin Sequencing (ATAC-seq) of Cancer Cells in Culture


Kaitlyn Gura et al.

The Assay for Transposase-Accessible Chromatin followed by sequencing (ATAC-seq) is a powerful and widely-used technique for chromatin accessibility profiling due to its low input requirement, simple protocol, high sensitivity, and ability to study single cells. ATAC-seq is a powerful tool in cancer epigenetics research that has enabled the scrutiny of gene regulatory mechanisms, aided the identification of therapeutic targets, and in the exploration of anticancer immunity, thereby advancing our understanding of cancer biology. The protocol includes five main steps: cell isolation and nuclei preparation, Tn5 tagmentation, PCR amplification, library sequencing, and data analysis. Here, we have outlined a comprehensive ATAC-seq protocol that is utilized by our laboratories, along with detailed troubleshooting steps at each point, in the hopes that it will aid other researchers in utilizing this tool to the fullest capability. We also describe bioinformatics pipelines for processing the raw sequence data and identifying regulatory regions by differential accessibility analysis, as well as more advanced methods for the visualization of transcription factor binding sites.

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Tagmentase

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Published
July, 2026

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Products used in this publication

  • Standardized Tagmentase Product Image
    C01070013-200
    Tagmentase (Tn5 transposase) – loaded
  • Kit icon
    C01019043
    Tagmentation Buffer (2x)
  • Kit icon
    C01011034
    24 UDI for Tagmented libraries - Set I
  • Kit icon
    C01011036
    24 UDI for tagmented libraries - Set II
  • default alt
    C01011037
    24 UDI for tagmented libraries - Set III