H3K36 Methylation - a Guardian of Epigenome Integrity
ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 164 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
- Mus musculus (mouse)
- Samples
- 164 samples: 128 distinct titles, 30 of them repeatedGroups 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
- H3K36 Methylation as a Guardian of Epigenome IntegrityNature communications · 2025
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.
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.
Supplementary files
The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE274367_RAW.tar (it can run to tens of gigabytes).
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 PRJNA1146045 and SRA study SRP525143. Searching any of these in the dataset finder brings you back here.
How we read this: Read from 164 sample titles: 128 distinct titles with little repetition. 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.
- GSM8447879 C3H10T1-2_H3K36M_ChIPseq_H3K27me1_batch1
- GSM8447880 C3H10T1-2_H3K36M_ChIPseq_H3K27me2_batch1
- GSM8447881 C3H10T1-2_H3K36M_ChIPseq_input_batch1
- GSM8447882 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_H3K27ac_rep1_batch2
- GSM8447883 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_H3K27ac_rep2_batch2
- GSM8447884 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_H3K27ac_rep3_batch2
- GSM8447885 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_H3K4me3_rep1_batch2
- GSM8447886 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_H3K4me3_rep2_batch2
- GSM8447887 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_H3K4me3_rep3_batch2
- GSM8447888 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_input_rep1_batch2
- GSM8447889 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_input_rep2_batch2
- GSM8447890 C3H10T1-2_NSD1-2-3-SETD2-ASH1L-QuiKO_ChIPseq_input_rep3_batch2
- GSM8447891 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_H3K27ac_rep1_batch2
- GSM8447892 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_H3K27ac_rep2_batch2
- GSM8447893 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_H3K27ac_rep3_batch2
- GSM8447894 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_H3K4me3_rep1_batch2
- GSM8447895 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_H3K4me3_rep2_batch2
- GSM8447896 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_H3K4me3_rep3_batch2
- GSM8447897 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_input_rep1_batch2
- GSM8447898 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_input_rep2_batch2
- GSM8447899 C3H10T1-2_NSD1-2-3-SETD2-QKO_ChIPseq_input_rep3_batch2
- GSM8447900 C3H10T1-2_NSD1-2-DKO_ChIPseq_H3K27me1_batch1
- GSM8447901 C3H10T1-2_NSD1-2-DKO_ChIPseq_H3K27me2_batch1
- GSM8447902 C3H10T1-2_NSD1-2-DKO_ChIPseq_H3K9me3_batch1
- GSM8447903 C3H10T1-2_NSD1-2-DKO_ChIPseq_input_batch1
- GSM8447904 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K27ac_rep1_batch2
- GSM8447905 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K27ac_rep2_batch2
- GSM8447906 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K27ac_rep3_batch2
- GSM8447907 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K27me1_batch1
- GSM8447908 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K27me2_batch1
- GSM8447909 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K27me3_batch1
- GSM8447910 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K4me3_rep1_batch2
- GSM8447911 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K4me3_rep2_batch2
- GSM8447912 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K4me3_rep3_batch2
- GSM8447913 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_H3K9me3_batch1
- GSM8447914 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_input_batch1
- GSM8447915 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_input_rep1-2_batch2
- GSM8447916 C3H10T1-2_NSD1-2-SETD2-TKO_ChIPseq_input_rep3_batch2
- GSM8447917 C3H10T1-2_Parental_ChIPseq_H3K27ac_rep1_batch2
- GSM8447918 C3H10T1-2_Parental_ChIPseq_H3K27ac_rep2_batch2
+ 124 more — browse all 164 samples with per-sample file links →
- GSE278068 Nanobody-tethered transposition for dual profiling of chromatin accessibility and DNA methylation 201 samples shares methylation
- GSE169102 DNA methyltransferase 1 modulates mitochondrial function through bridging m5C RNA methylation 187 samples shares methylation
- GSE289193 Histone H4 lysine 20 tri-methylation safeguards breast cancer lineage fidelity and unfolded protein response 160 samples shares methylation
- GSE71403 Tumor hypoxia causes DNA hypermethylation by reducing TET activity 99 samples shares methylation
- GSE261788 AMAR-seq: automated multimodal sequencing of DNA methylation, chromatin accessibility, and RNA expression with single-cell resolution 83 samples shares methylation
- GSE54365 High-resolution mapping reveals a conserved, widespread, dynamic meiotically regulated mRNA methylation program 76 samples shares methylation
- GSE291013 Methylation pseudotime analysis for label-free profiling of the temporal chromatin landscape with long-read and single-molecule resolution 62 samples shares methylation
- GSE51239 DNA methylation dynamics of the human pre-implantation embryo 48 samples shares methylation
Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.