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Omics Research//Single-Cell Sequencing

Single-Cell Epi ATAC Sequencing

Experience Epi ATAC-seq with improved sensitivity and nuclei recovery.

What Is Single-Cell ATAC-Seq?

Single-cell Assay for Transposase-Accessible Chromatin (Epi ATAC) sequencing is used to characterize chromatin states in individual cells. This is different from bulk ATAC sequencing, which provides an average readout of chromatin states in all cells in a sample.

For heterogeneous samples and sub-populations, single-cell is a more accurate, informative choice.



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Why Is ATAC-Seq Important?

ATAC sequencing is useful for identifying open chromatin regions. These regions are typically associated with active transcription factors impacting phenotype or disease states.

Single-cell ATAC-seq provides another level of specificity and differentiation. In tumor, tissue, and other heterogeneous samples, single-cell ATAC sequencing can map the epigenetic profiles of unique cell groups.

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About the Technology

10x Genomics Chromium X10x Genomics Chromium X

The Chromium X instrument simplifies, automates, and scales single-cell sequencing projects with proprietary cell partitioning and reagent delivery technologies. Downstream analysis is simplified with unique barcodes for each cell partition. 

More on the Chromium X →

Multiome GEM-Based Sequencing

10x Genomics’ GEM-based sequencing makes it possible to study complex biological samples at single-cell resolution. This technology keeps each cell’s genetic material uniquely labeled from the start of the project.

Nuclei are combined with barcoded gel beads and partitioned into tiny oil droplets called Gel Beads-in-Emulsion (GEMs), where lysis and molecular tagging happen in parallel. Inside each GEM, nucleic acids are tagged with a unique barcode, so all sequencing reads can later be traced back to their original cell.Screenshot 2026-04-16 at 10.30.42 AM

After the droplets are broken , two libraries are prepared (ATAC, 3`GEX), and next-generation sequencing is performed. The barcodes enable researchers to reconstruct a high-resolution view of gene expression, chromatin accessibility, or immune profiles, cell by cell.

About the Workflow

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DNA Fragmentation

Transposase enzyme is added to suspension; single nuclei in suspension are first transposed.

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Partitioning

A GEM encapsulates each reaction within the Chromium system.

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Barcoding

Transposed DNA fragments are distinguished with one of approximately 750,000 barcodes.

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Library Construction

The resulting library is used for scATAC-seq. In Epi multiome ATAC, two libraries are generated for scATAC-seq and 3` gene expression.

Epi ATAC Services at Psomagen

Simultaneously profile the transcriptome and epigenome. With scATAC seq coupled with single cell 3’ gene expression from the same cell, you can decipher what gene expression is occurring and determine how the structure of that DNA may regulate that expression.



The availability of chromatin for interaction with proteins, namely transcription factors, using the Assay for Transposase Accessible Chromatin, is a critical area of regulatory pathway discovery.

Using advanced microfluidics, Chromium instruments encapsulate Gel Beads in GEMs, or a “Gel Bead-in-emulsion,” along with a single cell or nucleus and reagents to create a micro-reaction.