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A trimeric USP11-USP7-TCEAL1 complex stabilizes paused RNAPII to sustain oncogenic transcription

GSE273326 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 63 samples Submitted 2025/04/25 Platform GPL30173
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 63 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
63 samples: 12 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
The USP11/TCEAL1 complex promotes transcription elongation to sustain oncogenic gene expression in neuroblastomaGenes & development · 2025
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
The USP11/TCEAL1 complex promotes transcription elongation to sustain oncogenic gene expression in neuroblastoma
Dehmer M, Trunk K, Gallant P et al. · Genes & development 2025 · PMID 40250979 · doi:10.1101/gad.352166.124
This dataset
Download · which file do I need?

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.

1 · Just have a look

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.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE273326_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

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 PRJNA1141426 and SRA study SRP522809. Searching any of these in the dataset finder brings you back here.

Study design
12 conditions, mostly in triplicate
RNAseq_MYCNER_shTCEAL1_Ctrl ×3 RNAseq_MYCNER_shTCEAL1_OHT ×3 RNAseq_MYCNER_shTCEAL1_Dox ×3 RNAseq_MYCNER_shTCEAL1_OHT_Dox ×3 RNAseq_MYCNER_shUSP11_Ctrl ×3 RNAseq_MYCNER_shUSP11_Dox ×3 RNAseq_MYCNER_shUSP11_siUSP7_Ctrl ×3 RNAseq_SHEP_siNTC ×3 +32 more

Supports a between-group comparison across 35 samples.

How we read this: 12 replicated groups read from 63 sample titles; they account for 35 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.

Samples in this study

+ 23 more — browse all 63 samples with per-sample file links →

Datasets on a similar topic

Search all human RNA-seq datasets in GEO →

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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.