Physical and functional interaction among Irf8 enhancers during dendritic cell differentiation
ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 89 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
- 89 samples: 29 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.
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 GSE239952_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 PRJNA1001813 and SRA study SRP452481. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 87 samples.
How we read this: 29 replicated groups read from 89 sample titles; they account for 87 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.
- GSM7670689 WT_MDP_H3K27ac_rep1 WT_MDP_H3K27ac
- GSM7670690 WT_MDP_H3K27ac_rep2 WT_MDP_H3K27ac
- GSM7670691 WT_MDP_H3K27ac_rep3 WT_MDP_H3K27ac
- GSM7670692 WT_CDP_H3K27ac_rep1 WT_CDP_H3K27ac
- GSM7670693 WT_CDP_H3K27ac_rep2 WT_CDP_H3K27ac
- GSM7670694 WT_CDP_H3K27ac_rep3 WT_CDP_H3K27ac
- GSM7670695 WT_cDC1_H3K27ac_rep1 WT_cDC1_H3K27ac
- GSM7670696 WT_cDC1_H3K27ac_rep2 WT_cDC1_H3K27ac
- GSM7670697 WT_cDC1_H3K27ac_rep3 WT_cDC1_H3K27ac
- GSM7670698 WT_in vitro_MDP_H3K27ac_rep1 WT_in vitro_MDP_H3K27ac
- GSM7670699 WT_in vitro_MDP_H3K27ac_rep2 WT_in vitro_MDP_H3K27ac
- GSM7670700 WT_in vitro_MDP_H3K27ac_rep3 WT_in vitro_MDP_H3K27ac
- GSM7670701 WT_in vitro_CDP_H3K27ac_rep1 WT_in vitro_CDP_H3K27ac
- GSM7670702 WT_in vitro_CDP_H3K27ac_rep2 WT_in vitro_CDP_H3K27ac
- GSM7670703 WT_in vitro_CDP_H3K27ac_rep3 WT_in vitro_CDP_H3K27ac
- GSM7670704 WT_in vitro_pre-cDC1_H3K27ac_rep1 WT_in vitro_pre-cDC1_H3…
- GSM7670705 WT_in vitro_pre-cDC1_H3K27ac_rep2 WT_in vitro_pre-cDC1_H3…
- GSM7670706 WT_in vitro_pre-cDC1_H3K27ac_rep3 WT_in vitro_pre-cDC1_H3…
- GSM7670707 WT_in vitro_cDC1_H3K27ac_rep1 WT_in vitro_cDC1_H3K27ac
- GSM7670708 WT_in vitro_cDC1_H3K27ac_rep2 WT_in vitro_cDC1_H3K27ac
- GSM7670709 WT_in vitro_cDC1_H3K27ac_rep3 WT_in vitro_cDC1_H3K27ac
- GSM7670710 d+56het_cDC1_H3K27ac_rep1 d+56het_cDC1_H3K27ac
- GSM7670711 d+56het_cDC1_H3K27ac_rep2 d+56het_cDC1_H3K27ac
- GSM7670712 d+56het_cDC1_H3K27ac_rep3 d+56het_cDC1_H3K27ac
- GSM7670713 d+56het_in vitro_pre-cDC1_H3K27ac_rep1 d+56het_in vitro_pre-cD…
- GSM7670714 d+56het_in vitro_pre-cDC1_H3K27ac_rep2 d+56het_in vitro_pre-cD…
- GSM7670715 d+56het_in vitro_pre-cDC1_H3K27ac_rep3 d+56het_in vitro_pre-cD…
- GSM7670716 d+32het_cDC1_H3K27ac_rep1 d+32het_cDC1_H3K27ac
- GSM7670717 d+32het_cDC1_H3K27ac_rep2 d+32het_cDC1_H3K27ac
- GSM7670718 d+32het_cDC1_H3K27ac_rep3 d+32het_cDC1_H3K27ac
- GSM7670719 d+32het_in vitro_pre-cDC1_H3K27ac_rep1 d+32het_in vitro_pre-cD…
- GSM7670720 d+32het_in vitro_pre-cDC1_H3K27ac_rep2 d+32het_in vitro_pre-cD…
- GSM7670721 d+32het_in vitro_pre-cDC1_H3K27ac_rep3 d+32het_in vitro_pre-cD…
- GSM7670722 WT_cDC1_MSCV_rep1 WT_cDC1_MSCV
- GSM7670723 WT_cDC1_MSCV_rep2 WT_cDC1_MSCV
- GSM7670724 WT_cDC1_MSCV_rep3 WT_cDC1_MSCV
- GSM7670725 d+56_cDC1_IRF8_rep1 d+56_cDC1_IRF8
- GSM7670726 d+56_cDC1_IRF8_rep2 d+56_cDC1_IRF8
- GSM7670727 d+56_cDC1_IRF8_rep3 d+56_cDC1_IRF8
- GSM7670728 d+32_cDC1_IRF8_rep1 d+32_cDC1_IRF8
+ 49 more — browse all 89 samples with per-sample file links →
- GSE326309 Cohesin complex cooperates with PU.1 at super-enhancers to regulate the differentiation and identity of conventional dendritic cells 34 samples shares enhancers, dendritic
- GSE269676 3D genome of CD8+ T cells reveals IRF8-mediated exhaustion in cancer 18 samples shares irf8
- GSE333230 The Transcription Factor IRF8 drives tumor-specific exhaustion in CD8 T cells 12 samples shares irf8
- GSE283421 C/EBP⍺ activates Irf8 expression in myeloid progenitors at the +56 kb 10 samples shares irf8
- GSE299305 3D genome of CD8+ T cells reveals IRF8-mediated exhaustion in cancer [Hi-C] 4 samples shares irf8
- GSE237916 Regulation of T helper cell differentiation by the interplay between histone modification and chromatin interaction 197 samples shares interaction
- GSE290849 Acute intervention reveals critical roles of BAF, KMT2D and p300 in MyoD binding on enhancers 143 samples shares enhancers
- GSE271298 Cohesin-mediated chromatin organization controls the differentiation and function of dendritic cells 103 samples shares dendritic
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.