Metastatic site influences driver gene function in pancreatic cancer
ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 75 samples
- What it is
- ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
- Organism
- Mus musculus (mouse)
- Samples
- 75 samples: 21 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
- SMAD4 induces opposite effects on metastatic growth from pancreatic tumors depending on the organ of residenceNature cancer · 2025
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.
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.
Supplementary files
The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE245827_RAW.tar (it can run to tens of gigabytes).
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: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.
Also filed as BioProject PRJNA1030027 and SRA study SRP467415. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 57 samples.
How we read this: 21 replicated groups read from 75 sample titles; they account for 57 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.
- GSM7849476 Panc-Smad4OFF_m1 Panc-Smad4OFF_m
- GSM7849477 Panc-Smad4OFF_m2 Panc-Smad4OFF_m
- GSM7849478 Panc-Smad4OFF_m3 Panc-Smad4OFF_m
- GSM7849479 Panc-Smad4ON_m1 Panc-Smad4ON_m
- GSM7849480 Panc-Smad4ON_m2 Panc-Smad4ON_m
- GSM7849481 Panc-Smad4ON_m3 Panc-Smad4ON_m
- GSM7849482 Liv-Smad4OFF_m1 Liv-Smad4OFF_m
- GSM7849483 Liv-Smad4OFF_m2 Liv-Smad4OFF_m
- GSM7849484 Liv-Smad4ON_m1 Liv-Smad4ON_m
- GSM7849485 Liv-Smad4ON_m2 Liv-Smad4ON_m
- GSM7849486 Lung-Smad4OFF_m1 Lung-Smad4OFF_m
- GSM7849487 Lung-Smad4OFF_m2 Lung-Smad4OFF_m
- GSM7849488 Lung-Smad4OFF_m3 Lung-Smad4OFF_m
- GSM7849489 Lung-Smad4ON_m1 Lung-Smad4ON_m
- GSM7849490 Lung-Smad4ON_m2 Lung-Smad4ON_m
- GSM7849491 Lung-Smad4ON_m3 Lung-Smad4ON_m
- GSM7849492 Panc-d7-Smad4OFF_m1 Panc-d7-Smad4OFF_m
- GSM7849493 Panc-d7-Smad4OFF_m2 Panc-d7-Smad4OFF_m
- GSM7849494 Panc-d7-Smad4OFF_m3 Panc-d7-Smad4OFF_m
- GSM7849495 Panc-d7-Smad4ON_m1 Panc-d7-Smad4ON_m
- GSM7849496 Panc-d7-Smad4ON_m2 Panc-d7-Smad4ON_m
- GSM7849497 Liv-d7-Smad4OFF_m1 Liv-d7-Smad4OFF_m
- GSM7849498 Liv-d7-Smad4OFF_m2 Liv-d7-Smad4OFF_m
- GSM7849499 Liv-d7-Smad4ON_m1 Liv-d7-Smad4ON_m
- GSM7849500 Liv-d7-Smad4ON_m2 Liv-d7-Smad4ON_m
- GSM7849501 Liv-d7-Smad4ON_m3 Liv-d7-Smad4ON_m
- GSM7849502 Lung-d7-Smad4OFF_m1 Lung-d7-Smad4OFF_m
- GSM7849503 Lung-d7-Smad4OFF_m2 Lung-d7-Smad4OFF_m
- GSM7849504 Lung-d7-Smad4OFF_m3 Lung-d7-Smad4OFF_m
- GSM7849505 Lung-d7-Smad4OFF_m4 Lung-d7-Smad4OFF_m
- GSM7849506 Lung-d7-Smad4ON_m1 Lung-d7-Smad4ON_m
- GSM7849507 Lung-d7-Smad4ON_m2 Lung-d7-Smad4ON_m
- GSM7849508 Panc-d14-Smad4OFF_m1 Panc-d14-Smad4OFF_m
- GSM7849509 Panc-d14-Smad4OFF_m2 Panc-d14-Smad4OFF_m
- GSM7849510 Panc-d14-Smad4ON_m1 Panc-d14-Smad4ON_m
- GSM7849511 Panc-d14-Smad4ON_m2 Panc-d14-Smad4ON_m
- GSM7849512 Panc-d14-Smad4ON_m3 Panc-d14-Smad4ON_m
- GSM7849513 Liv-d14-Smad4OFF_m1 Liv-d14-Smad4OFF_m
- GSM7849514 Liv-d14-Smad4OFF_m2 Liv-d14-Smad4OFF_m
- GSM7849515 Liv-d14-Smad4OFF_m3 Liv-d14-Smad4OFF_m
+ 35 more — browse all 75 samples with per-sample file links →
- GSE245821 Metastatic site influences driver gene function in pancreatic cancer [ATAC-seq] 16 samples shares metastatic, influences, pancreatic, driver, site
- GSE304622 KDM8 is a master regulator for hypoxia-induced metastatic heterogeneity in pancreatic cancer 43 samples shares metastatic, pancreatic
- GSE220556 In vivo CRISPR screens reveal SCAF1 and USP15 as novel drivers of pancreatic cancer 20 samples shares pancreatic, driver
- GSE270915 The expression order determines the pioneer functions of Ngn3 and NeuroD1 in pancreatic endocrine differentiation 3745 samples shares pancreatic
- GSE255278 Mediator Subunit MED4 Enforces Metastatic Dormancy in Breast Cancer 27 samples shares metastatic
- GSE271053 A forward genetic screen identifies Sirtuin1 as a driver of neuroendocrine prostate cancer [RNA-Seq] 43 samples shares driver
- GSE308709 Cellular and Spatial Drivers of Unresolved Injury Link to Functional Decline in the Human Kidney 36 samples shares driver
- GSE275728 Transcriptome analysis of pancreatic cancer cells with genetically modified Ptges or Ptger4 36 samples shares pancreatic
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.