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RNAseq of RPE-hTert cells expressing different levels of predictive reporter construct

GSE222337 Homo sapiens (human) RNA-seq (gene expression) 50 samples Submitted 2024/06/11 Platform GPL20301
At a glance

RNA-seq (gene expression) · human · 50 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)
Samples
50 samples: 10 conditions, mostly with about 5 replicates eachGroups 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
Titration of RAS alters senescent state and influences tumour initiationNature · 2024
Summary (written by the submitters)
RNAseq of different subpopulations of RPE1 cells expressing predictive reporter construct, pre- and on Day 6 post-induction with 4OHT
Published in
Titration of RAS alters senescent state and influences tumour initiation
Chan ASL, Zhu H, Narita M et al. · Nature 2024 · PMID 39112713 · doi:10.1038/s41586-024-07797-z
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 GSE222337_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: 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 PRJNA919036 and SRA study SRP416197. Searching any of these in the dataset finder brings you back here.

Study design
10 conditions, mostly with about 5 replicates each
L_d0 ×5 L_d6 ×5 M_d0 ×5 M_d6 ×5 N_d0 ×5 N_d6 ×5 S_d0 ×5 S_d6 ×5 +2 more

Supports a between-group comparison across 50 samples.

How we read this: 10 replicated groups read from 50 sample titles; they account for 50 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

+ 10 more — browse all 50 samples with per-sample file links →

Datasets on a similar topic

Search all human RNA-seq datasets in GEO →

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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.