Single-nucleus transcriptomics and chromatin accessibility of cell type-specific contributions to the epileptogenic cortex of focal cortical dysplasia type IIIa
Single-nucleus RNA-seq · human · 14 samples
- What it is
- Single-nucleus RNA-seqGene activity measured in individual nuclei (used when whole cells are hard to isolate, for example from frozen tissue).
- Organism
- Homo sapiens (human)
- Samples
- 14 samples: 4 × ATAC temporal neocortex, epileptogenic, vs 4 × RNA temporal neocortex, epileptogenic, vs 3 × ATAC temporal neocortex, nonepileptic, vs 3 × RNA temporal neocortex, nonepileptic,Groups 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
- Excitatory neurons and oligodendrocyte precursor cells are vulnerable to focal cortical dysplasia type IIIa as suggested by single-nucleus multiomicsClinical and translational medicine · 2024
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 GSE266308_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: Single-cell studies usually ship their counts as 10x files (matrix.mtx, barcodes.tsv, features.tsv), an .h5 file, or an .rds / .h5ad object that Seurat or Scanpy can open. Look for those among the supplementary files.
Also filed as BioProject PRJNA1106533 and SRA study SRP505058. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 14 samples.
How we read this: 4 replicated groups read from 14 sample titles; they account for 14 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.
- GSM8244645 ATAC temporal neocortex, nonepileptic,replicate1 ATAC temporal neocortex…
- GSM8244646 ATAC temporal neocortex, nonepileptic,replicate2 ATAC temporal neocortex…
- GSM8244647 ATAC temporal neocortex, nonepileptic,replicate3 ATAC temporal neocortex…
- GSM8244648 ATAC temporal neocortex, epileptogenic,replicate1 ATAC temporal neocortex…
- GSM8244649 ATAC temporal neocortex, epileptogenic,replicate2 ATAC temporal neocortex…
- GSM8244650 ATAC temporal neocortex, epileptogenic,replicate3 ATAC temporal neocortex…
- GSM8244651 ATAC temporal neocortex, epileptogenic,replicate4 ATAC temporal neocortex…
- GSM8244661 RNA temporal neocortex, nonepileptic,replicate1 RNA temporal neocortex,…
- GSM8244662 RNA temporal neocortex, nonepileptic,replicate2 RNA temporal neocortex,…
- GSM8244663 RNA temporal neocortex, nonepileptic,replicate3 RNA temporal neocortex,…
- GSM8244664 RNA temporal neocortex, epileptogenic,replicate1 RNA temporal neocortex,…
- GSM8244665 RNA temporal neocortex, epileptogenic,replicate2 RNA temporal neocortex,…
- GSM8244666 RNA temporal neocortex, epileptogenic,replicate3 RNA temporal neocortex,…
- GSM8244667 RNA temporal neocortex, epileptogenic,replicate4 RNA temporal neocortex,…
- GSE278910 Pooled CRISPR screens with joint single-nucleus chromatin accessibility and transcriptome profiling [CUT&RUN] 30 samples shares single-nucleus, accessibility, chromatin
- GSE254244 Cancer cell type-specific derepression of transposable elements by inhibition of chromatin modifier enzymes 112 samples shares type-specific, chromatin
- GSE329420 Endothelial exosomes remodel chromatin accessibility and superenhancer in cancer cells to promote liver metastatic colonization 26 samples shares accessibility, chromatin
- GSE277922 Chromatin Accessibility Analysis Reveals Regulatory Dynamics in hESC-Derived Kidney Organoids 25 samples shares accessibility, chromatin
- GSE309354 Inflammatory signaling differentially changes chromatin accessibility and gene expression of the PD- associated kinase LRRK2 between human and mice [multiome] 24 samples shares accessibility, chromatin
- GSE299702 [RelA ChIP-seq]: Characterization of transcriptional and chromatin accessibility landscape of human bronchial epithelial cells treated with synergistic immunostimulatory ligands. 13 samples shares accessibility, chromatin
- GSE251754 Simultaneous profiling of full-length RNA transcripts and chromatin accessibility within single cells of human retinal organoids 10 samples shares accessibility, chromatin
- GSE264684 Genetic effects on chromatin accessibility uncover mechanisms of liver gene regulation and quantitative traits 477 samples shares accessibility, chromatin
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.