Ectopic expression of DNMT3L in human trophoblast stem cells restores features of the placental methylome [ChIP-seq]
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 15 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
- 15 samples: 15 samples, each with a distinct title — no replicated groupsGroups 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
- Ectopic expression of DNMT3L in human trophoblast stem cells restores features of the placental methylomeCell stem cell · 2025
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 GSE266194_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 PRJNA1106286 and SRA study SRP504846. Searching any of these in the dataset finder brings you back here.
Any grouping that defines a comparison lives in the sample characteristics, which GEO records separately from the titles.
How we read this: Read from 15 sample titles: 15 distinct titles with little repetition. 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.
- GSM8242190 BTS11_1_H3K36me3
- GSM8242191 BTS11_1_H3K4me3
- GSM8242192 BTS11_1_H3K27me3
- GSM8242193 BTS11_1_H3K9me3
- GSM8242194 BTS11_1_Input
- GSM8242195 BTS11_2_H3K4me3
- GSM8242196 BTS11_2_H3K27me3
- GSM8242197 BTS11_2_H3K9me3
- GSM8242198 BTS11_2_Input
- GSM8242199 CT29_1_H3K4me3
- GSM8242200 CT29_1_H3K27me3
- GSM8242201 CT29_1_H3K9me3
- GSM8242202 CT29_2_H3K4me3
- GSM8242203 CT29_2_H3K27me3
- GSM8242204 CT29_2_H3K9me3
- GSE266196 Ectopic expression of DNMT3L in human trophoblast stem cells restores features of the placental methylome. 45 samples shares dnmt3l, trophoblast, placental, methylome, restores, features, ectopic
- GSE278374 PPARG-centric transcriptional re-wiring during differentiation of human trophoblast stem cells into extravillous trophoblasts [ChIP-seq] 44 samples shares trophoblast, chip-seq
- GSE295569 PPARG-centric transcriptional re-wiring during differentiation of human trophoblast stem cells into extravillous trophoblasts [ChIP-seq] 15 samples shares trophoblast, chip-seq
- GSE311483 BAP1 dysregulation impairs trophoblast differentiation and contributes to placental dysfunction in preeclampsia 32 samples shares trophoblast, placental
- GSE277759 Tumor suppresson protein p53 governs human trophoblast lineage development II 24 samples shares trophoblast
- GSE272427 SWI/SNF complex ATPase activity supports normal syncytiotrophoblast differentiation and shields from EVT differentiation [ATAC-seq] 20 samples shares trophoblast
- GSE202272 METTL3 regulates chromatin of human trophoblasts 14 samples shares trophoblast
- GSE56046 Transcriptomics and methylomics of human monocytes [methylome] 1202 samples shares methylome
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.