SKP1A-mediated degradation of PRC2 triggers activation of Polycomb-silenced genes : CUT&Tag 2
ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 12 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
- 12 samples: 6 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.
Read the full summary ↓
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 GSE263265_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 PRJNA1070432 and SRA study SRP486550. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 12 samples.
How we read this: 6 replicated groups read from 12 sample titles; they account for 12 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.
- GSM8188850 CT_9.0dpc_mb_RING1Blot1 CT_9.0dpc_mb_RING1Blot
- GSM8188851 CT_9.0dpc_mb_RING1Blot2 CT_9.0dpc_mb_RING1Blot
- GSM8188852 CTinput_9.5dpc_mb_RING1Blot1 CTinput_9.5dpc_mb_RING1…
- GSM8188853 CTinput_9.5dpc_mb_RING1Blot2 CTinput_9.5dpc_mb_RING1…
- GSM8188854 CT_9.5dpcPI_mb_RING1Blot1 CT_9.5dpcPI_mb_RING1Blot
- GSM8188855 CT_9.5dpcPI_mb_RING1Blot2 CT_9.5dpcPI_mb_RING1Blot
- GSM8188856 CT_9.5dpc_mb_RING1Blot1 CT_9.5dpc_mb_RING1Blot
- GSM8188857 CT_9.5dpc_mb_RING1Blot2 CT_9.5dpc_mb_RING1Blot
- GSM8188858 CTinput_9.0dpc_mb_RING1Blot1 CTinput_9.0dpc_mb_RING1…
- GSM8188859 CTinput_9.0dpc_mb_RING1Blot2 CTinput_9.0dpc_mb_RING1…
- GSM8188860 CTinput_9.5dpcPI_mb_RING1Blot1 CTinput_9.5dpcPI_mb_RIN…
- GSM8188861 CTinput_9.5dpcPI_mb_RING1Blot2 CTinput_9.5dpcPI_mb_RIN…
- GSE297309 SKP1A-mediated degradation of PRC2 triggers activation of Polycomb-silenced gene [CUT&Tag] 108 samples shares prc2, cut, polycomb-silenced, skp1a-mediated, degradation, activation, triggers
- GSE293160 SKP1A-mediated degradation of PRC2 triggers activation of Polycomb-silenced gene [RNA-seq] 24 samples shares prc2, polycomb-silenced, skp1a-mediated, degradation, activation, triggers
- GSE289642 Noncanonical PRC2 chromatin association reveals a key role of EZHIP in intergenerational epigenetic memory transition [ChIP-Seq, Cut & Run] 107 samples shares prc2, cut
- GSE325799 KMT2C and KMT2D amplify GRHL2-driven enhancer activation [CUT&Tag] 80 samples shares cut, activation
- GSE298002 Stage-specific Epigenetic Priming Amplifies Gene Activation During Lineage Commitment [CUT&Run] 38 samples shares cut, activation
- GSE279279 KDM6A facilitates Xist upregulation at the onset of X inactivation [CUT&Run] 14 samples shares cut, activation
- GSE219083 G-quadruplex folding in Xist RNA antagonizes PRC2 activity for step-wise regulation of X-chromosome inactivation 36 samples shares prc2, activation
- GSE274493 The remodeling of bivalent chromatin is essential for mouse peri-implantation embryogenesis [CUT&Tag] 46 samples shares cut
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.