The USP11/TCEAL1 complex promotes transcription elongation to sustain oncogenic gene expression in neuroblastoma [RNA-seq II]
RNA-seq (gene expression) · human · 21 samples
- What it is
- RNA-seq (gene expression)Gene activity measured by sequencing. The summary does not mention single-cell work, so this is most likely bulk: one average per sample, the usual starting point for comparing groups.
- Organism
- Homo sapiens (human)
- Topic
- NeuroblastomaThis series is part of our curated briefing on it.
- Samples
- 21 samples: 7 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
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 GSE294526_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: For RNA-seq the counts are usually a table among the supplementary files (look for 'counts', 'expression', 'FPKM' or 'TPM' in the file name). The series matrix of a sequencing study is sometimes nearly empty.
Also filed as BioProject PRJNA1250445 and SRA study SRP578404. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 21 samples.
How we read this: 7 replicated groups read from 21 sample titles; they account for 21 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.
- GSM8908482 RNAseq_MYCNER_shUSP11_Ctrl_rep1 RNAseq_MYCNER_shUSP11_C…
- GSM8908483 RNAseq_MYCNER_shUSP11_Ctrl_rep2 RNAseq_MYCNER_shUSP11_C…
- GSM8908484 RNAseq_MYCNER_shUSP11_Ctrl_rep3 RNAseq_MYCNER_shUSP11_C…
- GSM8908485 RNAseq_MYCNER_shUSP11_Dox_rep1 RNAseq_MYCNER_shUSP11_D…
- GSM8908486 RNAseq_MYCNER_shUSP11_Dox_rep2 RNAseq_MYCNER_shUSP11_D…
- GSM8908487 RNAseq_MYCNER_shUSP11_Dox_rep3 RNAseq_MYCNER_shUSP11_D…
- GSM8908488 RNAseq_MYCNER_shUSP11_siUSP7_Ctrl_rep1 RNAseq_MYCNER_shUSP11_s…
- GSM8908489 RNAseq_MYCNER_shUSP11_siUSP7_Ctrl_rep2 RNAseq_MYCNER_shUSP11_s…
- GSM8908490 RNAseq_MYCNER_shUSP11_siUSP7_Ctrl_rep3 RNAseq_MYCNER_shUSP11_s…
- GSM8908491 RNAseq_SHEP_siNTC_rep1 RNAseq_SHEP_siNTC
- GSM8908492 RNAseq_SHEP_siNTC_rep2 RNAseq_SHEP_siNTC
- GSM8908493 RNAseq_SHEP_siNTC_rep3 RNAseq_SHEP_siNTC
- GSM8908494 RNAseq_SHEP_siTCEAL1_rep1 RNAseq_SHEP_siTCEAL1
- GSM8908495 RNAseq_SHEP_siTCEAL1_rep2 RNAseq_SHEP_siTCEAL1
- GSM8908496 RNAseq_SHEP_siTCEAL1_rep3 RNAseq_SHEP_siTCEAL1
- GSM8908497 RNAseq_IMR5_siNTC_rep1 RNAseq_IMR5_siNTC
- GSM8908498 RNAseq_IMR5_siNTC_rep2 RNAseq_IMR5_siNTC
- GSM8908499 RNAseq_IMR5_siNTC_rep3 RNAseq_IMR5_siNTC
- GSM8908500 RNAseq_IMR5_siTCEAL1_rep1 RNAseq_IMR5_siTCEAL1
- GSM8908501 RNAseq_IMR5_siTCEAL1_rep2 RNAseq_IMR5_siTCEAL1
- GSM8908502 RNAseq_IMR5_siTCEAL1_rep3 RNAseq_IMR5_siTCEAL1
- GSE16476 Integrated bioinformatic and wet-lab approach to identify potential oncogenic networks in neuroblastoma 88 samples same disease briefing · shares neuroblastoma, oncogenic
- GSE164456 Histone lysine demethylase 4 family proteins maintain the transcriptional program and adrenergic cellular state of MYCN-amplified neuroblastoma 69 samples same disease briefing · shares transcription, neuroblastoma
- GSE183729 Single-cell MultiOmics and spatial transcriptomics demonstrate neuroblastoma developmental plasticity 18 samples same disease briefing · shares neuroblastoma
- GSE178937 RNA sequencing of neuroblastoma cells treated with selinexor or with XPO1 knockdown 12 samples same disease briefing · shares neuroblastoma
- GSE275538 Identification of EPLIN as a novel MYCN-independent target in neuroblastoma and medulloblastoma 1 samples same disease briefing · shares neuroblastoma
- GSE120572 A mechanistic classification of clinical phenotypes in neuroblastoma 394 samples same disease briefing · shares neuroblastoma
- GSE181582 IGF2BP1 induces neuroblastoma via a druggable feedforward loop with MYCN promoting 17q oncogene expression 264 samples same disease briefing · shares neuroblastoma
- GSE12494 SNP data from Neuroblastoma samples 262 samples same disease briefing · shares neuroblastoma
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.