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IRF4 requires ARID1A to establish plasma cell identity in multiple myeloma

GSE253716 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 99 samples Submitted 2024/05/01 Platform GPL30173Platform GPL11154Platform GPL30172
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 99 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)
Topic
Multiple myelomaThis series is part of our curated briefing on it.
Samples
99 samples: 46 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.
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
This dataset
Open GSE253716 in finder → Find more RNA-seq datasets → Multiple myeloma landscape →
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.

Series matrix ↓
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 GSE253716_RAW.tar (it can run to tens of gigabytes).

All supplementary files ↗ Whole study · RAW.tar ↓
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.

Raw reads on ENA ↗

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 PRJNA1066800 and SRA study SRP484757. Searching any of these in the dataset finder brings you back here.

NCBI GEO page ↗
Study design
46 conditions, mostly in duplicate
GCB ARID1A ×3 PC ARID1A ×3 SKMM1 4 hours (ATAC2) DMSO ×2 SKMM1 4 hours (ATAC2) FHD286 ×2 SKMM1 4 hours (ATAC2) combination ×2 NCIH929 4 hours (ATAC2) DMSO ×2 NCIH929 4 hours (ATAC2) FHD286 ×2 NCIH929 4 hours (ATAC2) combination ×2 +43 more

Supports a between-group comparison across 94 samples.

How we read this: 46 replicated groups read from 99 sample titles; they account for 94 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

+ 59 more — browse all 99 samples with per-sample file links →

More Multiple myeloma datasets

Search all RNA-seq datasets in GEO →

Share this dataset

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.