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RNA-seq of HeLa cells and RPE1 cells after USP39 KD using RNAi

GSE229329 Homo sapiens (human) RNA-seq (gene expression) 12 samples Submitted 2024/12/27 Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 12 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
12 samples: 3 × RNA-seq, HeLa, USP39, Ctrl, vs 3 × RNA-seq, HeLa, USP39, KD, vs 3 × RNA-seq_RPE_Ctrl vs 3 × RNA-seq_RPE_USP39_KDGroups 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
Pathogenic proteotoxicity of cryptic splicing is alleviated by ubiquitination and ER-phagyScience (New York, N.Y.) · 2024
Summary (written by the submitters)
We used HeLa cells and RPE1 cells after knockdown (KD) of USP39 using siRNAs. We compared differential expression and alternative splicing between Control and KD cells.
Published in
Pathogenic proteotoxicity of cryptic splicing is alleviated by ubiquitination and ER-phagy
Prieto-Garcia C, Matkovic V, Mosler T et al. · Science (New York, N.Y.) 2024 · PMID 39541449 · doi:10.1126/science.adi5295
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 GSE229329_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 PRJNA954019 and SRA study SRP431817. Searching any of these in the dataset finder brings you back here.

Study design
3 × RNA-seq, HeLa, USP39, Ctrl, vs 3 × RNA-seq, HeLa, USP39, KD, vs 3 × RNA-seq_RPE_Ctrl vs 3 × RNA-seq_RPE_USP39_KD

Supports a between-group comparison across 12 samples.

How we read this: 4 replicated groups read from 12 sample titles; they account for 12 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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