← BioTransfer GEO Dataset Finder
GEO series

RNA-Seq analysis LPCAT3 knockdown effect on primary human endometrial stromal cells(HESC).

GSE274335 Homo sapiens (human) RNA-seq (gene expression) 6 samples Submitted 2026/08/08 Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 6 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
6 samples: 3 × HESCs, siLPCAT3, vs 3 × HESCs, siNC,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.
Summary (written by the submitters)
Decidualization of human endometrial stromal cells (HESCs) is a critical process in the establishment of uterine receptivity and successful pregnancy. It involves profound cellular and molecular changes, including alterations in energy metabolism, which are necessary to support the increased metabolic demands of the decidualizing cells.
Read the full summary ↓
The enzyme lysophosphatidylcholine acyltransferase 3 (LPCAT3), known for its role in lipid remodeling, is hypothesized to influence the metabolic shifts occurring during HESC decidualization. To explore this hypothesis, we employed RNA sequencing (RNA-Seq) to assess the transcriptomic changes in HESCs following LPCAT3 knockdown during the decidualization process.
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 GSE274335_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 PRJNA1145986 and SRA study SRP525088. Searching any of these in the dataset finder brings you back here.

Study design
3 × HESCs, siLPCAT3, vs 3 × HESCs, siNC,

Supports a between-group comparison across 6 samples.

How we read this: 2 replicated groups read from 6 sample titles; they account for 6 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

Search all human RNA-seq datasets in GEO →

Share this dataset

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.