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      <image:title>Knowledge Center - Spatial CUT&amp;amp;Tag: High-Resolution Chromatin Profiling with Spatial Context​ - Make it stand out</image:title>
      <image:caption>Introduction Spatial CUT&amp;Tag enables high-resolution mapping of histone modifications and chromatin-associated proteins directly within intact tissue, preserving native architecture while revealing regulatory patterns that bulk methods cannot capture. Developed in the Fan Lab and published in Science, the method delivers reproducible, low-background chromatin profiles with strong concordance to ENCODE ChIP-seq. This white paper highlights how Spatial CUT&amp;Tag uncovers spatially distinct regulatory states—such as tumor-specific chromatin features and localized enhancer activity—to provide deeper insight into tissue heterogeneity and disease biology.</image:caption>
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      <image:caption>This case study demonstrates how AtlasXomics Spatial CoProfiling simultaneously captures chromatin accessibility (ATAC) and whole-transcriptome RNA expression from the same tissue section, preserving spatial context for regulatory inference. Using fresh-frozen mouse cerebellum, the analysis reveals distinct cellular architectures, strong accessibility–expression correlations for active regulatory programs, and clear examples where chromatin and RNA diverge to indicate poised or alternative regulatory states. These results highlight how Spatial CoProfiling enables researchers to interrogate regulatory logic in situ—connecting epigenomic state to transcriptional output with spatial precision.</image:caption>
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      <image:caption>This case study highlights how AtlasXomics’ in-situ bulk qualification assay (AtlasVerify) provides a high throughput method to evaluate FFPE tissue suitability before committing to a full spatial ATAC-seq run. Using an FFPE pancreatic neuroendocrine tumor sample, the workflow generated nucleosome-free profiles, TSS enrichment, FRiP scores, and IGV peak traces that accurately predicted the performance of the downstream spatial assay. The spatial ATAC results closely mirrored the bulk QC metrics—demonstrating matched chromatin accessibility patterns, strong fragment counts, and clear pathology-aligned clusters. This predictive QC step empowers researchers to select the right samples, reduce failure risk, and confidently advance their spatial studies.</image:caption>
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      <image:caption>Whatever it is, the way you tell your story online can make all the difference.</image:caption>
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      <image:caption>Whatever it is, the way you tell your story online can make all the difference.</image:caption>
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      <image:caption>Whatever it is, the way you tell your story online can make all the difference.</image:caption>
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    <loc>https://www.atlasxomics.com/june-newsletter/spatial-atac-seq-uncovers-glial-epigenetic-alterations-in-early-alzheimers-disease-slaxd-cmh4x</loc>
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      <image:title>June Newsletter - EpiTrace: A Chromatin Clock to Map Cell Mitotic Age from scATAC‑seq - Fig. 1. a) Schematic of mitotic-age tracing via chromatin accessibility (ChrAcc) at ClockDML sites. b) DNAm on G8-group ClockDML inversely correlates with PBMC age (R = −0.98, P &lt; 2.2 × 10⁻¹⁶; 95 % CI shaded). c) Enrichment odds ratios for mitosis-ClockDML, chronology-ClockDML and solo-WCGW loci across ATAC-seq peak sets from pan-cancer, bladder, normal, placenta and hematopoietic samples (Fisher’s exact test; whiskers = 95 % CI). d) Outline of the EpiTrace algorithm. e) UMAP of single-cell ATAC from early human embryos, colored by stage. f) ClockDML accessibility (raw and HMM-smoothed) and iterative EpiTrace age ranks across stages (sample counts in legend). Pearson correlations shown; P values &lt; 2.2 × 10⁻¹⁶ reported. “tropho.” = trophoblast.</image:title>
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      <image:title>June Newsletter - Spatial ATAC-seq Unmasks Early Glial Rewiring in Alzheimer’s - Fig. 1. Experimental workflow and key findings from spatial ATAC-seq in 5×FAD and control mouse brains. (A) Schematic of the experimental design. Spatial ATAC-seq was performed on sagittal brain sections from 5×FAD and C57BL/6J mice to profile chromatin accessibility across defined brain regions. (B) Key findings from the study include: (1) identification of major brain cell types and glial subtypes; (2) region-specific chromatin accessibility patterns; (3) cell-type-specific transcription factor motif enrichment; (4) differential chromatin accessibility in AD risk genes; and (5) experimental validation of Vsir expression in microglial subtypes.</image:title>
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    <lastmod>2025-06-12</lastmod>
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      <image:title>June Newsletter - Chromosome-Scale Shifts, Not Single Genes, Ignite Medulloblastoma - Clonal proliferation and differentiation gradients are independent of oncogene expression</image:title>
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      <image:title>June Newsletter - Chromatin Accessibility Flags GSTM1 as an Early Prognostic Marker in Glioblastoma&amp;nbsp; - Integrative chromatin and expression profiling highlights GSTM1 as a potential tumor biomarker</image:title>
      <image:caption>By combining ATAC-seq and RNA-seq analyses across tumor vs. normal and short- vs. long-survival patient samples, the authors identified 11 genes with both elevated promoter accessibility and gene expression. GSTM1 emerged as the top candidate, showing the strongest upregulation across conditions. Heatmaps of RNA and ATAC-seq data further confirmed its prominence, and representative ATAC-seq tracks highlighted markedly higher accessibility at the GSTM1 locus in short-survival samples compared to long-survival and normal tissues.</image:caption>
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