Distinct interactions between pioneer factor Ascl1/E12a and nucleosomes drive cell fate transitions
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 63 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
- 63 samples: 20 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.
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 GSE299971_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 PRJNA1277758 and SRA study SRP592332. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 60 samples.
How we read this: 20 replicated groups read from 63 sample titles; they account for 60 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.
- GSM9049852 ChIP_Ascl1_WT_D2_rep1 ChIP_Ascl1_WT_D2
- GSM9049853 ChIP_Ascl1_WT_D2_rep2 ChIP_Ascl1_WT_D2
- GSM9049854 ChIP_Ascl1_WT_D2_rep3 ChIP_Ascl1_WT_D2
- GSM9049855 Input_Ascl1_WT_D2_rep1 Input_Ascl1_WT_D2
- GSM9049856 Input_Ascl1_WT_D2_rep2 Input_Ascl1_WT_D2
- GSM9049857 Input_Ascl1_WT_D2_rep3 Input_Ascl1_WT_D2
- GSM9049858 ChIP_Ascl1_allRs_D2_rep1 ChIP_Ascl1_allRs_D2
- GSM9049859 ChIP_Ascl1_allRs_D2_rep2 ChIP_Ascl1_allRs_D2
- GSM9049860 ChIP_Ascl1_allRs_D2_rep3 ChIP_Ascl1_allRs_D2
- GSM9049861 Input_Ascl1_allRs_D2_rep1 Input_Ascl1_allRs_D2
- GSM9049862 Input_Ascl1_allRs_D2_rep2 Input_Ascl1_allRs_D2
- GSM9049863 Input_Ascl1_allRs_D2_rep3 Input_Ascl1_allRs_D2
- GSM9049864 ChIP_Ascl1_AAA_D2_rep1 ChIP_Ascl1_AAA_D2
- GSM9049865 ChIP_Ascl1_AAA_D2_rep2 ChIP_Ascl1_AAA_D2
- GSM9049866 ChIP_Ascl1_AAA_D2_rep3 ChIP_Ascl1_AAA_D2
- GSM9049867 Input_Ascl1_AAA_D2_rep1 Input_Ascl1_AAA_D2
- GSM9049868 Input_Ascl1_AAA_D2_rep2 Input_Ascl1_AAA_D2
- GSM9049869 Input_Ascl1_AAA_D2_rep3 Input_Ascl1_AAA_D2
- GSM9049870 ChIP_Ascl1_QA_D2_rep1 ChIP_Ascl1_QA_D2
- GSM9049871 ChIP_Ascl1_QA_D2_rep2 ChIP_Ascl1_QA_D2
- GSM9049872 ChIP_Ascl1_QA_D2_rep3 ChIP_Ascl1_QA_D2
- GSM9049873 Input_Ascl1_QA_D2_rep1 Input_Ascl1_QA_D2
- GSM9049874 Input_Ascl1_QA_D2_rep2 Input_Ascl1_QA_D2
- GSM9049875 Input_Ascl1_QA_D2_rep3 Input_Ascl1_QA_D2
- GSM9049944 ATAC_Ascl1_WT_D0_rep1
- GSM9049945 ATAC_Ascl1_AAA_D0_rep1
- GSM9049946 ATAC_Ascl1_QA_D0_rep1
- GSM9049947 ATAC_Ascl1_WT_D2_rep1 ATAC_Ascl1_WT_D2
- GSM9049948 ATAC_Ascl1_allRs_D2_rep1 ATAC_Ascl1_allRs_D2
- GSM9049949 ATAC_Ascl1_AAA_D2_rep1 ATAC_Ascl1_AAA_D2
- GSM9049950 ATAC_Ascl1_QA_D2_rep1 ATAC_Ascl1_QA_D2
- GSM9049951 ATAC_Ascl1_WT_D2_rep2 ATAC_Ascl1_WT_D2
- GSM9049952 ATAC_Ascl1_allRs_D2_rep2 ATAC_Ascl1_allRs_D2
- GSM9049953 ATAC_Ascl1_AAA_D2_rep2 ATAC_Ascl1_AAA_D2
- GSM9049954 ATAC_Ascl1_QA_D2_rep2 ATAC_Ascl1_QA_D2
- GSM9049955 ATAC_Ascl1_WT_D2_rep3 ATAC_Ascl1_WT_D2
- GSM9049956 ATAC_Ascl1_allRs_D2_rep3 ATAC_Ascl1_allRs_D2
- GSM9049957 ATAC_Ascl1_AAA_D2_rep3 ATAC_Ascl1_AAA_D2
- GSM9049958 ATAC_Ascl1_QA_D2_rep3 ATAC_Ascl1_QA_D2
- GSM9049959 ATAC_Ascl1_WT_D4_rep1 ATAC_Ascl1_WT_D4
+ 23 more — browse all 63 samples with per-sample file links →
- GSE299923 Distinct interactions between pioneer factor Ascl1/E12a and nucleosomes drive cell fate transitions [ATAC-seq] 39 samples shares ascl1, e12a, interactions, nucleosomes, transitions, distinct, pioneer, factor
- GSE299920 Distinct interactions between pioneer factor Ascl1/E12a and nucleosomes drive cell fate transitions [ChIP-seq] 24 samples shares ascl1, e12a, interactions, nucleosomes, transitions, distinct, pioneer, factor
- GSE267711 Genome-wide rotational and translational phasing of nucleosomes with human transcription factors 54 samples shares nucleosomes, factor
- GSE266495 Genome-wide rotational and translational phasing of nucleosomes with human transcription factors [ChIP-exo] 48 samples shares nucleosomes, factor
- GSE300854 Collective unstructured interactions drive chromatin binding of transcription factors. [CUT&RUN] 40 samples shares interactions, factor
- GSE281743 Epigenetic Subtypes of High-Grade T1 Bladder Cancer Reveal Intra-Tumor Heterogeneity and Distinct Interactions with Tumor Microenvironment 41 samples shares interactions, distinct
- GSE251729 JMJD1C facilitates long distance genomic interactions by promoting condensates formation of key leukemic transcription factors in multiple AML cells 28 samples shares interactions, factor
- GSE269555 Targeting the oncohistone-ASCL1 axis disrupts plasticity and suppresses pediatric gliomas [CUT&RUN] 39 samples shares ascl1
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.