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LaminB1 DamID, RNA-seq and Genome-wide analysis of replication timing in RIF1 depleted preimplantation mouse embryos

GSE262791 Mus musculus (mouse) RNA-seq (gene expression) 468 samples Submitted 2025/03/18 Platform GPL17021Platform GPL24247
At a glance

RNA-seq (gene expression) · mouse · 468 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
468 samples: 12 conditions, mostly with about 72 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
RIF1 controls replication timing in early mouse embryos independently of lamina-associated nuclear organizationDevelopmental cell · 2025
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
RIF1 controls replication timing in early mouse embryos independently of lamina-associated nuclear organization
Nakatani T, Schauer T, Pal M et al. · Developmental cell 2025 · PMID 40262611 · doi:10.1016/j.devcel.2025.03.016
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 GSE262791_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 PRJNA1093385 and SRA study SRP498633. Searching any of these in the dataset finder brings you back here.

Study design
12 conditions, mostly with about 72 replicates each
siCont_8Cell ×72 siRif1_4Cell ×72 siCont_Morula ×72 siCont_4Cell ×64 siRif1_8Cell ×64 siRif1_4C ×16 siRif1_8C ×15 siCon_8C ×8 +4 more

Supports a between-group comparison across 400 samples.

How we read this: 12 replicated groups read from the first 400 of 468 sample titles; they account for 400 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

+ 428 more — browse all 468 samples with per-sample file links →

Datasets on a similar topic

Search all mouse 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.