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Accurate isoform quantification by joint short- and long-read RNA-sequencing

GSE271530 Homo sapiens (human) RNA-seq (gene expression) 12 samples Submitted 2024/07/10 Platform GPL34678Platform GPL21697
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: 2 × Differentiated (day 41) - long reads vs 2 × Differentiated (day 61) - long reads vs 2 × Differentiated (day 41) - short reads vs 2 × Differentiated (day 61) - short readsGroups 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
Accurate isoform quantification by joint short- and long-read RNA-sequencingbioRxiv : the preprint server for biology · 2024
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
Accurate isoform quantification by joint short- and long-read RNA-sequencing
Apostolides M, Choi B, Navickas A et al. · bioRxiv : the preprint server for biology 2024 · PMID 39026819 · doi:10.1101/2024.07.11.603067
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 GSE271530_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 PRJNA1132164 and SRA study SRP518114. Searching any of these in the dataset finder brings you back here.

Study design
2 × Differentiated (day 41) - long reads vs 2 × Differentiated (day 61) - long reads vs 2 × Differentiated (day 41) - short reads vs 2 × Differentiated (day 61) - short reads

Supports a between-group comparison across 8 samples.

How we read this: 4 replicated groups read from 12 sample titles; they account for 8 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
Datasets on a similar topic

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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.