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Genome-wide analysis of RUNX3 binding and histone modification alteration after RUNX3 Knock out

GSE198664 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 18 samples Submitted 2025/03/04 Platform GPL18460Platform GPL18573
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 18 samples

What it is
ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
Organism
Homo sapiens (human)
Samples
18 samples: 9 conditions, mostly in duplicateGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
Aberrant Upregulation of RUNX3 Activates Developmental Genes to Drive Metastasis in Gastric CancerCancer research communications · 2024
Summary (written by the submitters)
We analyzed histone modification changes at RUNX3 binding sites after RUNX3 knock-pit in HGC27 gastric cancer cell
Published in
Aberrant Upregulation of RUNX3 Activates Developmental Genes to Drive Metastasis in Gastric Cancer
Suda K, Okabe A, Matsuo J et al. · Cancer research communications 2024 · PMID 38240752 · doi:10.1158/2767-9764.CRC-22-0165
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE198664_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.

Also filed as BioProject PRJNA816429 and SRA study SRP364133. Searching any of these in the dataset finder brings you back here.

Study design
9 conditions, mostly in duplicate
HGC27_WT_Input ×2 HGC27_RUNX3KO_Input ×2 HGC27_WT_RUNX3 ×2 HGC27_WT_H3K27ac ×2 HGC27_RUNX3KO_H3K27ac ×2 HGC27_WT_H3K4me3 ×2 HGC27_RUNX3KO_H3K4me3 ×2 HGC27_WT_H3K4me1 ×2 +1 more

Supports a between-group comparison across 18 samples.

How we read this: 9 replicated groups read from 18 sample titles; they account for 18 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study
Datasets on a similar topic

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