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RSK1 is an exploitable dependency in myeloid malignancies [RNA-seq]

GSE228758 Homo sapiens (human) RNA-seq (gene expression) 16 samples Submitted 2024/11/14 Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 16 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
16 samples: 5 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.
Paper
RSK1 is an exploitable dependency in myeloproliferative neoplasms and secondary acute myeloid leukemiaNature communications · 2025
Summary (written by the submitters)
RSK1 is an exploitable dependency in myeloid malignancies
Published in
RSK1 is an exploitable dependency in myeloproliferative neoplasms and secondary acute myeloid leukemia
Kong T, Laranjeira ABA, Letson CT et al. · Nature communications 2025 · PMID 39820365 · doi:10.1038/s41467-024-55643-7
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 GSE228758_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 PRJNA951430 and SRA study SRP430505. Searching any of these in the dataset finder brings you back here.

Study design
5 conditions, mostly in duplicate
HEL DMSO ×2 HEL PMD ×2 MV4-11 DMSO ×2 MV4-11 PMD ×2 MV4-11 Quiz ×2 MPN CD14+ Mono 1 DMSO ×1 MPN CD14+ Mono 1 PMD ×1 MPN CD14+ Mono 2 DMSO ×1 +3 more

Supports a between-group comparison across 10 samples.

How we read this: 5 replicated groups read from 16 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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