Functional Characterization of Cooperating MGA Mutations in RUNX1::RUNX1T1 Acute Myeloid Leukemia [ATAC-seq]
ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 10 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
- 10 samples: 5 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
- Functional characterization of cooperating MGA mutations in RUNX1::RUNX1T1 acute myeloid leukemiaLeukemia · 2024
Read the full summary ↓
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 GSE253752_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 PRJNA1066868 and SRA study SRP484783. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 10 samples.
How we read this: 5 replicated groups read from 10 sample titles; they account for 10 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.
- GSM8027480 WT Molm13 cells Rep1 WT Molm13 cells
- GSM8027481 MGA-KO Molm13 cells Rep1 MGA-KO Molm13 cells
- GSM8027482 WT Molm13 cells Rep2 WT Molm13 cells
- GSM8027483 MGA-KO Molm13 cells Rep2 MGA-KO Molm13 cells
- GSM8027484 Mga(+/+) Mouse Rep1 Mga(+/+) Mouse
- GSM8027485 Mga(+/+) Mouse Rep2 Mga(+/+) Mouse
- GSM8027486 Mga(+/-) Mouse Rep1 Mga(+/-) Mouse
- GSM8027487 Mga(+/-) Mouse Rep2 Mga(+/-) Mouse
- GSM8027488 Mga(-/-) Mouse Rep1 Mga(-/-) Mouse
- GSM8027489 Mga(-/-) Mouse Rep2 Mga(-/-) Mouse
- GSE230265 The transcriptional co-repressor Runx1t1 is essential for N-Myc-driven neuroblastoma tumorigenesis 76 samples shares runx1t1, runx1
- GSE248948 Spatiotemporal control of SMARCA5 by a MAPK-RUNX1 axis distinguishes mutant KRAS-driven pancreatic malignancy from tissue regeneration 170 samples shares runx1
- GSE248947 Spatiotemporal control of SMARCA5 by a MAPK-RUNX1 axis distinguishes mutant KRAS-driven pancreatic malignancy from tissue regeneration (RNA-Seq) 28 samples shares runx1
- GSE267261 IRF2BP2 affects T-ALL cell proliferation by cooperating with master transcription factors [RNA-Seq] 9 samples shares cooperating
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.