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MARK2/MARK3 kinases are catalytic co-dependencies of YAP/TAZ in human cancer

GSE242517 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 192 samples Submitted 2024/07/19 Platform GPL30173Platform GPL21697
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 192 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
Homo sapiens (human)
Samples
192 samples: 62 conditions, mostly in duplicateGroups 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
MARK2/MARK3 Kinases Are Catalytic Codependencies of YAP/TAZ in Human CancerCancer discovery · 2024
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
MARK2/MARK3 Kinases Are Catalytic Codependencies of YAP/TAZ in Human Cancer
Klingbeil O, Skopelitis D, Tonelli C et al. · Cancer discovery 2024 · PMID 39058094 · doi:10.1158/2159-8290.CD-23-1529
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 GSE242517_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: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.

Also filed as BioProject PRJNA1013786 and SRA study SRP457503. Searching any of these in the dataset finder brings you back here.

Study design
62 conditions, mostly in duplicate
CUT&RUN MDA-MB231 H3K27ac d7 sgMARK2+3, ×3 CUT&RUN MDA-MB231 IgG d7 sgMARK2+3, ×3 RNA-seq A549_sgCtrl ×2 RNA-seq A549_sgM2_3 ×2 RNA-seq A549_sgY1T1 ×2 RNA-seq ASPC1_sgCtrl ×2 RNA-seq ASPC1_sgM2_3 ×2 RNA-seq ASPC1_sgY1T1 ×2 +120 more

Supports a between-group comparison across 126 samples.

How we read this: 62 replicated groups read from 192 sample titles; they account for 126 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

+ 152 more — browse all 192 samples with per-sample file links →

Datasets on a similar topic

Search all human ChIP / ATAC / CUT&Tag datasets in GEO →

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