Cancer-associated Histone H3 N-terminal arginine mutations disrupt PRC2 activity and impair differentiation
ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 79 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
- 79 samples: 25 conditions, mostly in triplicateGroups 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
- Cancer-associated Histone H3 N-terminal arginine mutations disrupt PRC2 activity and impair differentiationNature communications · 2024
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 GSE239638_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 PRJNA1000460 and SRA study SRP452444. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 75 samples.
How we read this: 25 replicated groups read from 79 sample titles; they account for 75 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.
- GSM7669106 H3WT__replicate_1 H3WT
- GSM7669107 H3WT__replicate_2 H3WT
- GSM7669108 H3WT__replicate_3 H3WT
- GSM7669109 H3R2C_replicate_1 H3R2C
- GSM7669110 H3R2C_replicate_2 H3R2C
- GSM7669111 H3R2C_replicate_3 H3R2C
- GSM7669112 H3R8C_replicate_1 H3R8C
- GSM7669113 H3R8C_replicate_2 H3R8C
- GSM7669114 H3R8C_replicate_3 H3R8C
- GSM7669115 H3R17C_replicate_1 H3R17C
- GSM7669116 H3R17C_replicate_2 H3R17C
- GSM7669117 H3R17C_replicate_3 H3R17C
- GSM7669118 H3R26C_replicate_1 H3R26C
- GSM7669119 H3R26C_replicate_2 H3R26C
- GSM7669120 H3R26C_replicate_3 H3R26C
- GSM7669159 H3WT_IgG_replicate_1 H3WT_IgG
- GSM7669160 H3WT_IgG_replicate_2 H3WT_IgG
- GSM7669161 H3WT_IgG_replicate_3 H3WT_IgG
- GSM7669162 H3WT_antiHA_replicate_1 H3WT_antiHA
- GSM7669163 H3WT_antiHA_replicate_2 H3WT_antiHA
- GSM7669164 H3WT_antiHA_replicate_3 H3WT_antiHA
- GSM7669165 H3WT_antiH3K4me3_replicate_1 H3WT_antiH3K4me3
- GSM7669166 H3WT_antiH3K4me3_replicate_2 H3WT_antiH3K4me3
- GSM7669167 H3WT_antiH3K4me3_replicate_3 H3WT_antiH3K4me3
- GSM7669168 H3WT_antiH3K27me3_replicate_1 H3WT_antiH3K27me3
- GSM7669169 H3WT_antiH3K27me3_replicate_2 H3WT_antiH3K27me3
- GSM7669170 H3WT_antiH3K27me3_replicate_3 H3WT_antiH3K27me3
- GSM7669171 H3R2C_IgG_replicate_1 H3R2C_IgG
- GSM7669172 H3R2C_IgG_replicate_2 H3R2C_IgG
- GSM7669173 H3R2C_IgG_replicate_3 H3R2C_IgG
- GSM7669174 H3R2C_antiHA_replicate_1 H3R2C_antiHA
- GSM7669175 H3R2C_antiHA_replicate_2 H3R2C_antiHA
- GSM7669176 H3R2C_antiHA_replicate_3 H3R2C_antiHA
- GSM7669177 H3R2C_antiH3K4me3_replicate_1 H3R2C_antiH3K4me3
- GSM7669178 H3R2C_antiH3K4me3_replicate_2 H3R2C_antiH3K4me3
- GSM7669179 H3R2C_antiH3K4me3_replicate_3 H3R2C_antiH3K4me3
- GSM7669180 H3R2C_antiH3K27me3_replicate_1 H3R2C_antiH3K27me3
- GSM7669181 H3R2C_antiH3K27me3_replicate_2 H3R2C_antiH3K27me3
- GSM7669182 H3R2C_antiH3K27me3_replicate_3 H3R2C_antiH3K27me3
- GSM7669183 H3R8C_IgG_replicate_1 H3R8C_IgG
+ 39 more — browse all 79 samples with per-sample file links →
- GSE239632 Cancer-associated Histone H3 N-terminal arginine mutations disrupt PRC2 activity and impair differentiation [RNA-Seq] 15 samples shares prc2, cancer-associated, n-terminal, mutations, arginine, activity, histone, disrupt
- GSE286459 The conserved N-terminal SANT1-binding domain (SBD) of EZH2 Regulates PRC2 Activity [delSBD-ChIP-Rx] 18 samples shares prc2, n-terminal, activity
- GSE286457 The conserved N-terminal SANT1-binding domain (SBD) of EZH2 Regulates PRC2 Activity [MTF2-JARID2] 15 samples shares prc2, n-terminal, activity
- GSE223666 Alternative splicing decouples local from global PRC2 activity 87 samples shares prc2, activity
- GSE310209 Opposing functions of AEBP2 isoforms fine-tune PRC2 catalytic activity 72 samples shares prc2, activity
- GSE219083 G-quadruplex folding in Xist RNA antagonizes PRC2 activity for step-wise regulation of X-chromosome inactivation 36 samples shares prc2, activity
- GSE306783 EPOP and MTF2 Activate PRC2 Activity through DNA-sequence specificity 34 samples shares prc2, activity
- GSE270581 Chromatin distribution alterations of histone modifacations and PRC2 complex caused by Rack7 deletion in primary astrocyte [ChIP-Seq] 24 samples shares prc2, histone
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.