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Autism spectrum disorder associated chromatin modifiers converge on transcription with sex-specific regulatory signatures

GSE286067 Mus musculus (mouse) RNA-seq (gene expression) 66 samples Submitted 2025/04/16 Platform GPL32159
At a glance

RNA-seq (gene expression) · mouse · 66 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
66 samples: 22 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.
Paper
Autism spectrum disorder risk genes have convergent effects on transcription and neuronal firing patterns in primary neuronsbioRxiv : the preprint server for biology · 2025
Summary (written by the submitters)
We sought to understand the transcriptional disruptions and functional impacts of the loss of 9 autism spectrum disorder (ASD) risk genes that encode transcriptional regulators in neurons. In addition to understanding how these signature converge or diverge, we aimed to study how sex could modulate these consequences.
Published in
Autism spectrum disorder risk genes have convergent effects on transcription and neuronal firing patterns in primary neurons
Paranjapye A, Ahmad R, Su S et al. · bioRxiv : the preprint server for biology 2025 · PMID 40196547 · doi:10.1101/2025.03.25.645337
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 GSE286067_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 PRJNA1207575 and SRA study SRP555888. Searching any of these in the dataset finder brings you back here.

Study design
22 conditions, mostly in triplicate
Neurons, No virus, male, ×3 Neurons, No virus, female, ×3 Neurons, Nontargetting Control, male, ×3 Neurons, Nontargetting Control, female, ×3 Neurons, Ash1l dep, male, ×3 Neurons, Ash1l dep, female, ×3 Neurons, Chd8 dep, male, ×3 Neurons, Chd8 dep, female, ×3 +14 more

Supports a between-group comparison across 66 samples.

How we read this: 22 replicated groups read from 66 sample titles; they account for 66 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

+ 26 more — browse all 66 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.