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Cyclic stretching stimuli promotes HGF and MMP secretion from hESC-derived hepatoblasts and endothelial cells towards liver lobule formation in vitro.

GSE232118 Homo sapiens (human) RNA-seq (gene expression) 15 samples Submitted 2024/05/10 Platform GPL18573
At a glance

RNA-seq (gene expression) · human · 15 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
15 samples: 5 × Day9 mixture, without cMS, vs 5 × Day12 mixture, without cMS, vs 5 × Day12 mixture, with cMS,Groups 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
Cyclic Stretching Enhances Angiocrine Signals at Liver Bud Stage from Human Pluripotent Stem Cells in Two-Dimensional CultureTissue engineering. Part A · 2024
Summary (written by the submitters)
We induced hepatic and endothelial cells simultaneously for day9. We applied cyclic mechancial stimuli (cMS) from day9 to day12. We then performed gene expression profiling analysis using data obtained from RNA-seq of 3 different cells at two time points.
Published in
Cyclic Stretching Enhances Angiocrine Signals at Liver Bud Stage from Human Pluripotent Stem Cells in Two-Dimensional Culture
Yoshimoto K, Maki K, Adachi T et al. · Tissue engineering. Part A 2024 · PMID 38062736 · doi:10.1089/ten.TEA.2023.0148
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 GSE232118_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 PRJNA970861 and SRA study SRP436759. Searching any of these in the dataset finder brings you back here.

Study design
5 × Day9 mixture, without cMS, vs 5 × Day12 mixture, without cMS, vs 5 × Day12 mixture, with cMS,

Supports a between-group comparison across 15 samples.

How we read this: 3 replicated groups read from 15 sample titles; they account for 15 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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