A Conserved Switch to Less Catalytically Active Polycomb Repressive Complexes in non-dividing cells
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 46 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
- 46 samples: 46 samples, each with a distinct title — no replicated groupsGroups 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
- A conserved switch to less catalytically active Polycomb repressive complexes in non-dividing cellsCell reports · 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 GSE200514_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 PRJNA824861 and SRA study SRP368322. Searching any of these in the dataset finder brings you back here.
Any grouping that defines a comparison lives in the sample characteristics, which GEO records separately from the titles.
How we read this: Read from 46 sample titles: 46 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.
- GSM6035345 quiescent_TIG3T_EZH1_ChIPRx
- GSM6035346 cycling_TIG3T_EZH1_ChIPRx
- GSM6041784 quiescent_TIG3T_EZH2_ChIPRx
- GSM6041785 quiescent_TIG3T_EED_ChIPRx
- GSM6041786 quiescent_TIG3T_CBX7_ChIPRx
- GSM6041787 quiescent_TIG3T_PHC1_ChIPRx
- GSM6041788 quiescent_TIG3T_H2AK119ub1_ChIPRx
- GSM6041789 cycling_TIG3T_EZH2_ChIPRx
- GSM6041790 cycling_TIG3T_EED_ChIPRx
- GSM6041791 cycling_TIG3T_CBX7_ChIPRx
- GSM6041792 cycling_TIG3T_PHC1_ChIPRx
- GSM6041793 cycling_TIG3T_H2AK119ub1_ChIPRx
- GSM6041794 quiescent_DMSO_TIG3T_EED_ChIPRx
- GSM6041795 quiescent_UNC6852_TIG3T_EED_ChIPRx
- GSM6041796 quiescent_DMSO_TIG3T_CBX7_ChIPRx
- GSM6041797 quiescent_UNC6852_TIG3T_CBX7_ChIPRx
- GSM6041798 quiescent_DMSO_TIG3T_H3K27me3_ChIPRx
- GSM6041799 quiescent_UNC6852_TIG3T_H3K27me3_ChIPRx
- GSM6041800 cycling_TIG3T_INPUT
- GSM6041801 quiescent_TIG3T_INPUT
- GSM6041802 quiescent_IMR90_H3K27me3_ChIPseq
- GSM6041803 quiescent_IMR90_H3K27me2_ChIPseq
- GSM6041804 quiescent_IMR90_H3K27me1_ChIPseq
- GSM6041805 cycling_IMR90_H3K27me3_ChIPseq
- GSM6041806 cycling_IMR90_H3K27me2_ChIPseq
- GSM6041807 cycling_IMR90_H3K27me1_ChIPseq
- GSM6041808 cycling_IMR90_INPUT
- GSM6041809 quiescent_IMR90_INPUT
- GSM6041810 quiescent_Rep1_RNAseq
- GSM6041811 quiescent_Rep2_RNAseq
- GSM6041812 cycling_Rep1_RNAseq
- GSM6041813 cycling_Rep2_RNAseq
- GSM6041814 quiescent_DMSO_R1_144h_Quantseq
- GSM6041815 quiescent_DMSO_R2_144h_Quantseq
- GSM6041816 quiescent_DMSO_R3_144h_Quantseq
- GSM6041817 quiescent_A395_R1_144h_Quantseq
- GSM6041818 quiescent_A395_R2_144h_Quantseq
- GSM6041819 quiescent_A395_R3_144h_Quantseq
- GSM6041820 AS_DMSO_R1_144h_Quantseq
- GSM6041821 AS_DMSO_R2_144h_Quantseq
+ 6 more — browse all 46 samples with per-sample file links →
- GSE291441 variant Polycomb Repressive complexes 1 (vPRC1s) in synovial sarcoma 16 samples shares repressive, complexes, polycomb
- GSE305426 DNA Hypomethylation is Not Cell Intrinsically Toxic to Polycomb Repressive Complex 2 Deficient Malignant Peripheral Nerve Sheath Tumors 36 samples shares repressive, polycomb
- GSE287322 Molecular signatures define BAP1-altered meningioma as a distinct CNS tumor with deregulation of Polycomb repressive complex target genes 29 samples shares repressive, polycomb
- GSE294307 5-hydroxymethylcytosine deposition mediates Polycomb Repressive Complex 2 function in MYCN-amplified neuroblastoma [CUT&Run] 18 samples shares repressive, polycomb
- GSE294304 5-hydroxymethylcytosine deposition mediates Polycomb Repressive Complex 2 function in MYCN-amplified neuroblastoma [nano-seal, 5hmC] 18 samples shares repressive, polycomb
- GSE294308 5-hydroxymethylcytosine deposition mediates Polycomb Repressive Complex 2 function in MYCN-amplified neuroblastoma [RNA-seq] 14 samples shares repressive, polycomb
- GSE314620 ORCA-mediated Polycomb Repressive Complex stabilization maintains 3D-genome architecture and controls replication timing [Cut & Run] 14 samples shares repressive, polycomb
- GSE341885 The catalytically inactive KDM5B-NTT isoform associates with chromatin and increases H3K4 trimethylation in breast cancer cells 13 samples shares catalytically, active
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.