Single nuclei chromatin accessibility and transcriptomic map of breast tissues of women of diverse genetic ancestry [10X single-cell multiome]
Single-nucleus RNA-seq · human · 32 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
- 32 samples: 32 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.
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 GSE244585_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 PRJNA1023624 and SRA study SRP464412. 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 32 sample titles: 32 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.
- GSM7821192 Ashkenazi_NormalBreastSample_multiome_Pool1, scATAC-seq
- GSM7821193 KTB_pool-3-Ashkenazi_jew, scATAC-seq
- GSM7821194 KTB_pool-4-Ashkenazi_jew, scATAC-seq
- GSM7821195 KTBpool5_Ashkenazi_jew, scATAC-seq
- GSM7821196 KTBpool6_Ashkenazi_jew, scATAC-seq
- GSM7821197 Pool7_BRCA2Positive, scATAC-seq
- GSM7821198 Pool8_BRCA1Positive, scATAC-seq
- GSM7821199 KTBpool9-White American, scATAC-seq
- GSM7821200 KTBpool11-White American, scATAC-seq
- GSM7821201 KTBpool12-White American, scATAC-seq
- GSM7821202 KTBpool_13-Indigenous American, scATAC-seq
- GSM7821203 KTBpool_14-Indigenous American, scATAC-seq
- GSM7821204 KTBpool15_Asian, scATAC-seq
- GSM7821205 KTBpool17_Asian, scATAC-seq
- GSM7821206 C23_KTBpool-23_Hispanic, scATAC-seq
- GSM7821207 C25_KTBpool-25_Hispanic, scATAC-seq
- GSM7821208 Ashkenazi_NormalBreastSample_multiome_Pool1, scRNA-seq
- GSM7821209 KTB_pool-3-Ashkenazi_jew, scRNA-seq
- GSM7821210 KTB_pool-4-Ashkenazi_jew, scRNA-seq
- GSM7821211 KTBpool5_Ashkenazi_jew, scRNA-seq
- GSM7821212 KTBpool6_Ashkenazi_jew, scRNA-seq
- GSM7821213 Pool7_BRCA2Positive, scRNA-seq
- GSM7821214 Pool8_BRCA1Positive, scRNA-seq
- GSM7821215 KTBpool9-White American, scRNA-seq
- GSM7821216 KTBpool11-White American, scRNA-seq
- GSM7821217 KTBpool12-White American, scRNA-seq
- GSM7821218 KTBpool_13-Indigenous American, scRNA-seq
- GSM7821219 KTBpool_14-Indigenous American, scRNA-seq
- GSM7821220 KTBpool15_Asian, scRNA-seq
- GSM7821221 KTBpool17_Asian, scRNA-seq
- GSM7821222 C23_KTBpool-23_Hispanic, scRNA-seq
- GSM7821223 C25_KTBpool-25_Hispanic, scRNA-seq
- GSE304741 Cytotoxic CD39+ tumor-associated NK cells respond to NKG2A blockade in lung cancer (10X Multiome) 22 samples shares 10x, multiome
- GSE274113 Transcription factor networks disproportionately enrich for heritability of blood cell phenotypes [10x ATAC + GEX Multiome] 42 samples shares 10x, multiome
- GSE303855 Mechanistic and Epigenetic Partitioning of Lamina-Associated Chromatin Revealed by a Genome-Wide Imaging Screen 45 samples shares chromatin, genetic
- GSE299348 Single-cell epigenetic, transcriptional, protein, and TCR states of HIV-1-infected cells in gut 117 samples shares single-cell, genetic
- GSE305146 Single-Cell Multiomic Atlas of Human Cortical Development in Down Syndrome - Fetal Cortex Multiome Dataset 92 samples shares single-cell, multiome
- GSE283621 Single-cell multi-omics analysis identifies metabolism-linked epigenetic reprogramming as a driver of therapy-resistant medulloblastoma 79 samples shares single-cell, genetic
- GSE316389 Chromatin accessibility and gene expression profiling of primary and metastatic ER+ breast cancer [ATAC-seq] 36 samples shares accessibility, chromatin
- GSE337246 Integrated single-cell profiling of RNA and DNA interactomes reveals targetable chromatin architectures in cancer [scRNA-Seq organoids] 35 samples shares single-cell, 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.