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Trajectory modeling of first trimester placenta highlight differences between cytotrophoblast progenitors and trophoblast stem cells

GSE270174 Homo sapiens (human) RNA-seq (gene expression) 50 samples Submitted 2024/08/16 Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 50 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
50 samples: 9 conditions, mostly with about 4 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
Single-cell transcriptomics reveal differences between chorionic and basal plate cytotrophoblasts and trophoblast stem cellsbioRxiv : 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
Single-cell transcriptomics reveal differences between chorionic and basal plate cytotrophoblasts and trophoblast stem cells
Morey R, Soncin F, Kallol S et al. · bioRxiv : the preprint server for biology 2024 · PMID 39071344 · doi:10.1101/2024.07.12.603155
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 GSE270174_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 PRJNA1125375 and SRA study SRP514626. Searching any of these in the dataset finder brings you back here.

Study design
9 conditions, mostly with about 4 replicates each
BP-CTB_1344 ×11 CP-CTB_1347 ×8 CP-CTB_1459 ×7 1815_d ×4 1816_d ×4 TSC, patient ×3 BP-CTB_1459 ×3 Basal Plate, patient ×2 +7 more

Supports a between-group comparison across 44 samples.

How we read this: 9 replicated groups read from 50 sample titles; they account for 44 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

+ 10 more — browse all 50 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.