NELF prevents transcriptional readthrough into DNA replication zones in cancer cells
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 70 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
- 70 samples: 35 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
- NELF prevents transcriptional readthrough into DNA replication zones in cancer cellsEMBO reports · 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 GSE253121_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 PRJNA1064075 and SRA study SRP483321. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 70 samples.
How we read this: 35 replicated groups read from 70 sample titles; they account for 70 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.
- GSM8012359 ATAC_0h_R1 ATAC_0h
- GSM8012360 ATAC_0h_R2 ATAC_0h
- GSM8012361 ATAC_4h_R1 ATAC_4h
- GSM8012362 ATAC_4h_R2 ATAC_4h
- GSM8012363 ATAC_24h_R1 ATAC_24h
- GSM8012364 ATAC_24h_R2 ATAC_24h
- GSM8012365 RNAseq_pA_0h_R1 RNAseq_pA_0h
- GSM8012366 RNAseq_pA_0h_R2 RNAseq_pA_0h
- GSM8012367 RNAseq_pA_4h_R1 RNAseq_pA_4h
- GSM8012368 RNAseq_pA_4h_R2 RNAseq_pA_4h
- GSM8012369 RNAseq_Nuclear_pA_0h_R1 RNAseq_Nuclear_pA_0h
- GSM8012370 RNAseq_Nuclear_pA_0h_R2 RNAseq_Nuclear_pA_0h
- GSM8012371 RNAseq_Nuclear_pA_4h_R1 RNAseq_Nuclear_pA_4h
- GSM8012372 RNAseq_Nuclear_pA_4h_R2 RNAseq_Nuclear_pA_4h
- GSM8012373 RNAseq_Nuclear_pA_12h_R1 RNAseq_Nuclear_pA_12h
- GSM8012374 RNAseq_Nuclear_pA_12h_R2 RNAseq_Nuclear_pA_12h
- GSM8012375 RNAseq_Nuclear_pA_24h_R1 RNAseq_Nuclear_pA_24h
- GSM8012376 RNAseq_Nuclear_pA_24h_R2 RNAseq_Nuclear_pA_24h
- GSM8014350 POINTseq_NELFC_0h_R1 POINTseq_NELFC_0h
- GSM8014351 POINTseq_NELFC_0h_R2 POINTseq_NELFC_0h
- GSM8014352 POINTseq_NELFC_4h_R1 POINTseq_NELFC_4h
- GSM8014353 POINTseq_NELFC_4h_R2 POINTseq_NELFC_4h
- GSM8014354 POINTseq_NELFC_0h_DMSO_R1 POINTseq_NELFC_0h_DMSO
- GSM8014355 POINTseq_NELFC_0h_DMSO_R2 POINTseq_NELFC_0h_DMSO
- GSM8014356 POINTseq_NELFC_4h_DMSO_R1 POINTseq_NELFC_4h_DMSO
- GSM8014357 POINTseq_NELFC_4h_DMSO_R2 POINTseq_NELFC_4h_DMSO
- GSM8014358 POINTseq_NELFC_0h_PlaB_R1 POINTseq_NELFC_0h_PlaB
- GSM8014359 POINTseq_NELFC_0h_PlaB_R2 POINTseq_NELFC_0h_PlaB
- GSM8014360 POINTseq_NELFC_4h_PlaB_R1 POINTseq_NELFC_4h_PlaB
- GSM8014361 POINTseq_NELFC_4h_PlaB_R2 POINTseq_NELFC_4h_PlaB
- GSM8014362 POINTseq_NELFE_0h_R1 POINTseq_NELFE_0h
- GSM8014363 POINTseq_NELFE_0h_R2 POINTseq_NELFE_0h
- GSM8014364 POINTseq_NELFE_4h_R1 POINTseq_NELFE_4h
- GSM8014365 POINTseq_NELFE_4h_R2 POINTseq_NELFE_4h
- GSM8014366 POINTseq_SPT4_0h_R1 POINTseq_SPT4_0h
- GSM8014367 POINTseq_SPT4_0h_R2 POINTseq_SPT4_0h
- GSM8014368 POINTseq_SPT4_3h_R1 POINTseq_SPT4_3h
- GSM8014369 POINTseq_SPT4_3h_R2 POINTseq_SPT4_3h
- GSM8014370 POINTseq_NELFC_0h_SIRV_R1 POINTseq_NELFC_0h_SIRV
- GSM8014371 POINTseq_NELFC_0h_SIRV_R2 POINTseq_NELFC_0h_SIRV
+ 30 more — browse all 70 samples with per-sample file links →
- GSE236553 CDK12 prevents MYC-induced transcription-replication conflicts 48 samples shares replication, prevents
- GSE293195 Regulated TRESLIN-MTBP loading governs initiation zones and replication timing in human DNA replication [ChIP-Seq] 46 samples shares replication, zones
- GSE236545 CDK12 prevents MYC-induced transcription-replication conflicts [RNA-seq] 14 samples shares replication, prevents
- GSE236550 CDK12 prevents MYC-induced transcription-replication conflicts [EdU-seq] 12 samples shares replication, prevents
- GSE236549 CDK12 prevents MYC-induced transcription-replication conflicts [EU-seq] 12 samples shares replication, prevents
- GSE338229 The combination of nelfinavir and cisplatin drives lytic cell death through a caspase-8/caspase-3/GSDME axis in platinum-resistant ovarian cancer cells 12 samples shares nelf
- GSE311396 NELFA-mediated promoter-proximal pausing restrains YAP-driven transcription and shapes context-dependent outcomes in breast cancer 12 samples shares nelf
- GSE318641 Dynamic interaction between tentacle-tethered microdomains in Integrator and NELF regulates the promoter-proximal pause checkpoint 61 samples shares nelf
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.