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Identifying STRN3-RARA as a new fusion gene for acute promyelocytic leukemia

GSE224816 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 22 samples Submitted 2024/04/23 Platform GPL24247Platform GPL24676
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 22 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)
Topic
Acute myeloid leukemiaThis series is part of our curated briefing on it.
Samples
22 samples: 8 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
Identifying STRN3-RARA as a new fusion gene for acute promyelocytic leukemiaBlood · 2023
Summary (written by the submitters)
Here we report a new fusion gene, STRN3-RARA, in acute promyelocytic leukemia (APL). It cooperates with UTX deficiency to drive full-blown APL in mice. Although STRN3-RARA leukemia quickly relapses after all-trans retinoic acid treatment, it can be restrained by cepharanthine.
Published in
Identifying STRN3-RARA as a new fusion gene for acute promyelocytic leukemia
Zhang Q, Li H, Chen X et al. · Blood 2023 · PMID 37624915 · doi:10.1182/blood.2023020619
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 GSE224816_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 PRJNA932745 and SRA study SRP424212. Searching any of these in the dataset finder brings you back here.

Study design
8 conditions, mostly in triplicate
RNAseq_pMIG ×3 RNAseq_sgUTX-pMIG ×3 RNAseq_sgUTX-S ×3 RNAseq_S ×3 CUTTAG_IgG ×2 CUTTAG_S ×2 RNAseq_Mouse_SR_ATRA ×2 RNAseq_Mouse_SR_Veh ×2 +2 more

Supports a between-group comparison across 20 samples.

How we read this: 8 replicated groups read from 22 sample titles; they account for 20 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
More Acute myeloid leukemia datasets

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