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Transcriptome profiling of ovaries in aged mice administered additional Samul-tang-associated compounds

GSE333820 Mus musculus (mouse) RNA-seq (gene expression) 96 samples Submitted 2026/07/06 Platform GPL19057
At a glance

RNA-seq (gene expression) · mouse · 96 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
Mus musculus (mouse)
Samples
96 samples: 30 conditions, mostly in triplicateGroups 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.
Summary (written by the submitters)
Samul-tang (SM) is a traditional multi-ingredient treatment widely used in clinical practice for women's health and reproductive disorders. Despite its therapeutic benefits, the complexity of its mechanisms of action due to the combination of multiple compounds has limited its research integration into modern pharmacological science. To address this challenge, we identified 28 herbal compounds as major ingredients in SM and generated transcriptome data from the mice ovaries after administrating with individual ingredients.
Read the full summary ↓
This dataset aims to provide insights into the mechanisms of action of SM and to aid in the identification of effective ingredient combinations.
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 GSE333820_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 PRJNA1472606 and SRA study SRP704890. Searching any of these in the dataset finder brings you back here.

Study design
30 conditions, mostly in triplicate
OC ×6 YC ×6 OC + Ethyl gallate ×3 OC + 5,7-Dimethoxycoumarin ×3 OC + Scoparone ×3 OC + 7-Methoxycoumarin ×3 OC + Decursinol ×3 OC + Bergaptol ×3 +22 more

Supports a between-group comparison across 96 samples.

How we read this: 30 replicated groups read from 96 sample titles; they account for 96 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

+ 56 more — browse all 96 samples with per-sample file links →

Datasets on a similar topic

Search all mouse 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.