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Stratifying IVF population endometria using a prognosis gradient independent of endometrial timing

GSE283409 Homo sapiens (human) RNA-seq (gene expression) 195 samples Submitted 2026/02/13 Platform GPL18573
At a glance

RNA-seq (gene expression) · human · 195 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
195 samples: 5 conditions, mostly with about 74 replicates eachGroups 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
A Drug Repurposing Strategy for a New Cause of Endometrial Infertility: Unveiling Promising New TreatmentsmedRxiv : the preprint server for health sciences · 2025
Summary (written by the submitters)
This study aimed to stratify and characterize the disrupted WOI patterns using endometrial timing-corrected whole gene expression and artificial intelligence (AI) models in in vitro fertilization (IVF) patients undergoing hormone replacement therapy (HRT).
Published in
A Drug Repurposing Strategy for a New Cause of Endometrial Infertility: Unveiling Promising New Treatments
Parraga-Leo A, Sebastian-Leon P, Sanchez-Reyes JM et al. · medRxiv : the preprint server for health sciences 2025 · PMID 41282672 · doi:10.1101/2025.11.04.25339037
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 GSE283409_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 PRJNA1193593 and SRA study SRP549109. Searching any of these in the dataset finder brings you back here.

Study design
5 conditions, mostly with about 74 replicates each
P ×74 V ×49 M ×26 B ×23 BI ×22 V37 ×1

Supports a between-group comparison across 194 samples.

How we read this: 5 replicated groups read from 195 sample titles; they account for 194 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

+ 155 more — browse all 195 samples with per-sample file links →

Datasets on a similar topic

Search all human 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.