Mapping breakome of multiple cancer cell-lines
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 62 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
- 62 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
- Superenhancers shape the landscape and repair dynamics of transcription-associated DNA breaks in cancerScience advances · 2026
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 GSE290558_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 PRJNA1228613 and SRA study SRP566479. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 59 samples.
How we read this: 21 replicated groups read from 62 sample titles; they account for 59 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.
- GSM8816539 A4098_rep1 A4098
- GSM8816540 A4098_rep2 A4098
- GSM8816541 A4098_rep3 A4098
- GSM8816542 HEK_293_rep1 HEK_293
- GSM8816543 HEK_293_rep2 HEK_293
- GSM8816544 HEK_293_rep3 HEK_293
- GSM8816545 HeLa_CDK9i_rep1 HeLa_CDK9i
- GSM8816546 HeLa_CDK9i_rep2 HeLa_CDK9i
- GSM8816547 HeLa_CDK9i_rep3 HeLa_CDK9i
- GSM8816548 HeLa_dBET6_rep1 HeLa_dBET6
- GSM8816549 HeLa_dBET6_rep2 HeLa_dBET6
- GSM8816550 HeLa_dBET6_rep3 HeLa_dBET6
- GSM8816551 HeLa_DMSO_rep1 HeLa_DMSO
- GSM8816552 HeLa_DMSO_rep2 HeLa_DMSO
- GSM8816553 HeLa_DMSO_rep3 HeLa_DMSO
- GSM8816554 HeLa_siSc_rep1 HeLa_siSc
- GSM8816555 HeLa_siSc_rep2 HeLa_siSc
- GSM8816556 HeLa_siXRCC4_rep1 HeLa_siXRCC4
- GSM8816557 HeLa_siXRCC4_rep2 HeLa_siXRCC4
- GSM8816558 HMLE_rep1 HMLE
- GSM8816559 HMLE_rep2 HMLE
- GSM8816560 HMLE_rep3 HMLE
- GSM8816561 HMLE_rep4 HMLE
- GSM8816562 MCF10A_rep1 MCF10A
- GSM8816563 MCF10A_rep2 MCF10A
- GSM8816564 MCF7_ATMi_ver1 MCF7_ATMi_ve
- GSM8816565 MCF7_ATMi_ver2 MCF7_ATMi_ve
- GSM8816566 MCF7_ATMi_ver3 MCF7_ATMi_ve
- GSM8816567 MCF7_CDK9i_rep1 MCF7_CDK9i
- GSM8816568 MCF7_CDK9i_rep2 MCF7_CDK9i
- GSM8816569 MCF7_CDK9i_rep3 MCF7_CDK9i
- GSM8816570 MCF7_cycling_rep1 MCF7_cycling
- GSM8816571 MCF7_cycling_rep2 MCF7_cycling
- GSM8816572 MCF7_dBET6_rep1 MCF7_dBET6
- GSM8816573 MCF7_dBET6_rep2 MCF7_dBET6
- GSM8816574 MCF7_dBET6_rep3 MCF7_dBET6
- GSM8816575 MCF7_DMSO_ATMi_rep1 MCF7_DMSO_ATMi
- GSM8816576 MCF7_DMSO_ATMi_rep2 MCF7_DMSO_ATMi
- GSM8816577 MCF7_DMSO_ATMi_rep3 MCF7_DMSO_ATMi
- GSM8816578 MCF7_DMSO_rep1 MCF7_DMSO
+ 22 more — browse all 62 samples with per-sample file links →
- GSE290554 Mapping the Molecular Signature of Progressive Multiple Sclerosis 94 samples shares multiple, mapping
- GSE290450 Mapping the Molecular Signature of Progressive Multiple Sclerosis [194017] 78 samples shares multiple, mapping
- GSE279180 Cell type mapping reveals tissue niches and interactions in subcortical multiple sclerosis lesions [snRNA-seq] 16 samples shares multiple, mapping
- GSE208732 Mapping functional to morphological variation reveals the basis of regional extracellular matrix subversion and nerve invasion in pancreatic cancer [RNA-seq] 102 samples shares mapping
- GSE266330 Single cell profiling of bone metastasis ecosystems from multiple cancer types reveals convergent and divergent mechanisms of bone colonization 63 samples shares multiple
- GSE310425 Transcriptome-wide mapping reveals an RNA-dependent mechanism of platinum cancer drugs 44 samples shares mapping
- GSE333379 AXL phosphosite mapping links FAK1 and YAP1 signaling to erlotinib resistance in EGFR-mutant lung cancer 29 samples shares mapping
- GSE261171 High-Resolution Single-Cell RNA Sequencing Uncovers Disparate Neutrophil Populations within Metastatic Cancer Lesions Linked to Progression Free Survival in Multiple Myeloma Patients 28 samples shares multiple
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.