
Spatial Epigenomics with Cellular Resolution
Map gene regulation in tissue like never before
AtlasXomics offers the first and only platform for high-resolution spatial epigenome mapping—combining spatial barcoding with ATAC-seq and CUT&Tag. Study gene regulation in intact tissues while preserving spatial context across cell types and regulatory states.
Designed for discovery in cancer, development, and aging, our platform helps you uncover the epigenetic mechanisms that drive disease—directly in situ. With intuitive kits and expert support, spatial epigenomics is now accessible to every lab.
Unique set of comprehensive spatial epigenomics solutions
Histology Image
Analyze a 5.5mm x 5.5mm region on a standard 1 x 3 inch pathology slide
Spatial ATAC-Seq
Maps open chromatin across tissue sections (gene regulatory regions)
Spatial CUT&Tag
Maps histone modifications or transcription factor binding in situ
AtlasXomics Public Data
Explore raw, downloadable datasets generated with AtlasXomics spatial epigenomics technologies. Browse a few highlights below or jump straight to the full Data Portal.
Epigenomic landscape of human dorsal root ganglion: sex differences & nociceptive gene regulation
Accessibility programs in hDRG highlighting transcriptional regulation across nociceptor populations.
View on Data Portal ↗Spatially organized cellular communities form the developing mouse heart
Chromatin accessibility across intact embryonic heart sections from early chamber formation to neonatal adaptation.
View on Data Portal ↗Distinct chromatin accessibility changes during yolk sac tumor infiltration
High-resolution mapping of accessibility and TF motifs in a germinoma-derived xenograft model.
View on Data Portal ↗Spatial profiling of chromatin accessibility reveals alteration of glial cells in Alzheimer’s disease mouse brain
Microenvironment-dependent accessibility shifts across AD-associated glial populations.
View on Data Portal ↗Spatial ATAC-seq mapping of gastric adenocarcinoma at 10 µm resolution
Tumor architecture preserved while profiling accessibility to uncover epigenetic mechanisms of heterogeneity.
View on Data Portal ↗