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Unraveling Hypoxia-Driven Gene and Methylation Signatures in Meningioma: Identifying Novel Biomarkers and Therapeutic Targets

GSE282352 Homo sapiens (human) DNA methylation 10 samples Submitted 2026/02/18 Platform GPL24676Platform GPL33022
At a glance

DNA methylation · human · 10 samples

What it is
DNA methylationChemical marks on DNA that help switch genes on or off.
Organism
Homo sapiens (human)
Samples
10 samples: 3 × IOMM-Lee norm_biol vs 3 × IOMM-Lee hyp_biol vs 2 × Normoxia EPIC V2, vs 2 × Hypoxia EPIC V2,Groups 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
Novel insights into hypoxia-driven transcriptomic and epigenetic landscapes in grade 3 meningiomaJournal of translational medicine · 2025
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
Novel insights into hypoxia-driven transcriptomic and epigenetic landscapes in grade 3 meningioma
Dalal M, Joshi R, Ajithkumar P et al. · Journal of translational medicine 2025 · PMID 41437098 · doi:10.1186/s12967-025-07606-9
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 GSE282352_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 beta-value tables or raw IDAT files among the supplementary files.

Also filed as BioProject PRJNA1188173 and SRA study SRP546254. Searching any of these in the dataset finder brings you back here.

Study design
3 × IOMM-Lee norm_biol vs 3 × IOMM-Lee hyp_biol vs 2 × Normoxia EPIC V2, vs 2 × Hypoxia EPIC V2,

Supports a between-group comparison across 10 samples.

How we read this: 4 replicated groups read from 10 sample titles; they account for 10 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
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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.