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A single-cell transcriptomic map of the human and mouse pancreas reveals inter- and intra-cell population structure

GSE84133 Homo sapiens (human) Single-cell RNA-seq 6 samples Submitted 2016/09/26 Platform GPL17021Platform GPL16791
At a glance

Single-cell RNA-seq · human · 6 samples

What it is
Single-cell RNA-seqGene activity measured in thousands of individual cells, so cell types can be told apart.
Organism
Homo sapiens (human)
Samples
6 samples
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.
Summary (written by the submitters)
While the function of the mammalian pancreas hinges on complex interactions of distinct cell types, gene expression profiles have primarily been described with bulk mixtures of cells. Here, we invoked inDrop, a droplet-based single-cell RNA-Seq method, to determine the transcriptomes of over 12,000 individual pancreatic cells from four human donors and two strains of mice.
Read the full summary ↓
Cells could be divided into 15 clusters that matched previously characterized cell types: all endocrine cell types, including rare ghrelin-expressing epsilon-cells, exocrine cell types, vascular cells, Schwann cells, quiescent and activated pancreatic stellate cells, and four types of immune cells. We detected subpopulations of ductal cells with distinct expression profiles, and validated their existence with immuno-histochemistry stains. Moreover, among human beta-cells, we detected heterogeneity in the regulation of genes relating to functional maturation and levels of ER-stress. Finally, we deconvolve bulk gene expression samples using single-cell RNA-Seq to detect disease associated differential expression. Thus, our cross-species dataset provides a resource for the discovery of novel cell type-specific and cell type-restricted transcription factors, signaling receptors, and medically-relevant genes.
This dataset
Download · which file do I need?

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.

1 · Just have a look

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.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE84133_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

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 PRJNA328774 and SRA study SRP078321. Searching any of these in the dataset finder brings you back here.

Samples in this study

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