← BioTransfer GEO Dataset Finder
GEO series

scRNA of the immune infiltrate of TRAMP-C1 allografts upon different androgen-deprivation therapeutic combinations

GSE272999 Mus musculus (mouse) Single-cell RNA-seq 10 samples Submitted 2024/08/21 Platform GPL19057
At a glance

Single-cell RNA-seq · mouse · 10 samples

What it is
Single-cell RNA-seqGene activity measured in thousands of individual cells, so cell types can be told apart.
Organism
Mus musculus (mouse)
Samples
10 samples: 8 distinct titles, 2 of them repeatedGroups 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
Coagulation factor X promotes resistance to androgen-deprivation therapy in prostate cancerCancer cell · 2024
Summary (written by the submitters)
Prostate cancer (PCa) is the second most frequent cancer diagnosis made in men and the fifth leading cause of death worldwide. Since PCa initiation and disease progression are driven by androgen receptor (AR) signaling, several effective AR signaling inhibitors (ARSIs) have been developed in the last few years. However, despite initial clinically significant therapy responses, secondary resistance to these treatments eventually emerges.
Read the full summary ↓
Therapy resistance in prostate cancer is commonly associated with inflammation and accumulation of immunosuppressive neutrophils in the tumor microenvironment, also secreting oncogenic factors.
Published in
Coagulation factor X promotes resistance to androgen-deprivation therapy in prostate cancer
Calì B, Troiani M, Bressan S et al. · Cancer cell 2024 · PMID 39303726 · doi:10.1016/j.ccell.2024.08.018
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 GSE272999_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 PRJNA1139771 and SRA study SRP521977. Searching any of these in the dataset finder brings you back here.

Study design
8 distinct titles, 2 of them repeated
ENZA_early ×2 antiIL23_early ×2

How we read this: Read from 10 sample titles: 8 distinct titles with little repetition. 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 mouse 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.