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Human ribomes reveal DNA-embedded ribonucleotides as epigenetic modulators of DNA supercoiling

GSE297046 Homo sapiens (human) DNA methylation 40 samples Submitted 2026/07/14 Platform GPL20795Platform GPL21697Platform GPL16791Platform GPL34284
At a glance

DNA methylation · human · 40 samples

What it is
DNA methylationChemical marks on DNA that help switch genes on or off.
Organism
Homo sapiens (human)
Samples
40 samples: 9 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.
Summary (written by the submitters)
The goal of this study is to analyze distribution and enrichment of ribonucleotide embedment in human genome in various genomic regions of funcitonal relevance and association with gene expression and methylation levels.
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 GSE297046_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 PRJNA1257959 and SRA study SRP583138. Searching any of these in the dataset finder brings you back here.

Study design
9 conditions, mostly in duplicate
Whole genome bisulfite-seq of CD4T ×4 ribose-seq of CD4T genomic DNA with dsF+RE1 f… ×3 ribose-seq of hESC-H9 genomic DNA with dsF fr… ×2 ribose-seq of HEK293T genomic DNA with dsF fr… ×2 ribose-seq of HEK293T RNase H2 KO (T3-8) geno… ×2 ribose-seq of HEK293T RNase H2 KO (T3-17) gen… ×2 RNA-seq of HEK293T-RNH2AKO-T3-17 ×2 RNA-seq of HEK293T-RNH2AKO-T3-8 ×2 +20 more

Supports a between-group comparison across 21 samples.

How we read this: 9 replicated groups read from 40 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.

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.