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HybriSeq: Probe-based Device-free Single-cell RNA Profiling

GSE292322 Homo sapiens (human) Single-cell RNA-seq 13 samples Submitted 2025/08/02 Platform GPL19969Platform GPL16417Platform GPL34328Platform GPL15520
At a glance

Single-cell RNA-seq · human · 13 samples

What it is
Single-cell RNA-seqGene activity measured in thousands of individual cells, so cell types can be told apart.
Organism
Homo sapiens (human)
Samples
13 samples: 3 × HEK293_37C vs 3 × HEK293_90C vs 2 × HEK293_Do-11-10Groups 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
HybriSeq: probe-based device-free single-cell RNA profilingCommunications biology · 2025
Summary (written by the submitters)
We have developed the HybriSeq method for single-cell RNA profiling, which utilizes in situ hybridization of multiple probes for targeted transcripts, followed by split-pool barcoding and sequencing analysis of the probes. We have shown that HybriSeq can achieve high sensitivity for RNA detection with multiple probes and profile entire transcripts without an end bias. The utility of HybriSeq is demonstrated in characterizing cell-to-cell heterogeneities of a panel of 196 genes in peripheral blood mononuclear cells and the detection of missed annotations of transcripts.
Published in
HybriSeq: probe-based device-free single-cell RNA profiling
Foyt D, Brown D, Zhou S et al. · Communications biology 2025 · PMID 40830572 · doi:10.1038/s42003-025-08702-8
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 GSE292322_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: Single-cell studies usually ship their counts as 10x files (matrix.mtx, barcodes.tsv, features.tsv), an .h5 file, or an .rds / .h5ad object that Seurat or Scanpy can open. Look for those among the supplementary files.

Also filed as BioProject PRJNA1237907 and SRA study SRP571418. Searching any of these in the dataset finder brings you back here.

Study design
3 × HEK293_37C vs 3 × HEK293_90C vs 2 × HEK293_Do-11-10

Supports a between-group comparison across 8 samples.

How we read this: 3 replicated groups read from 13 sample titles; they account for 8 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
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