Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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The transcriptional landscape of mouse blood stem/progenitor cell transitions at single cell resolution


ABSTRACT: Current gene-expression databases for the haematopoietic system provide information on gene expression profiles present in bulk populations. Although informative, these studies lack the resolution that can be gained at a single-cell level. In particular, population-average data assumes homogeneity within the population and may as such obscure the ability to detect the heterogeneity of decision-making processes in individual cells. Here we report 1656 single cell transcriptomes analysed by single-cell RNA sequencing. Cells were FACS sorted on broad gates encompassing haematopoietic stem and progenitor populations (HSPCs), with index sorting data collected to permit retrospective identification of populations by surface marker expression. Our dataset thus represents the gene expression landscape of HSPCs at single-cell resolution, capturing the heterogeneity in and between cell populations. Pseudotime analysis visualized haematopoietic stem (HSC) to progenitor transitions, identified HSC as well as lineage-specific transcriptional programs, and also highlighted putative lineage branching points. To provide access to the wider scientific community, a user-friendly website was developed with intuitive search and display functionality. Single cell RNA sequencing of haematopoeitic stem and progenitor cells

ORGANISM(S): Mus musculus

SUBMITTER: Evangelia Diamanti 

PROVIDER: E-GEOD-81682 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

A single-cell resolution map of mouse hematopoietic stem and progenitor cell differentiation.

Nestorowa Sonia S   Hamey Fiona K FK   Pijuan Sala Blanca B   Diamanti Evangelia E   Shepherd Mairi M   Laurenti Elisa E   Wilson Nicola K NK   Kent David G DG   Göttgens Berthold B  

Blood 20160630 8


Maintenance of the blood system requires balanced cell fate decisions by hematopoietic stem and progenitor cells (HSPCs). Because cell fate choices are executed at the individual cell level, new single-cell profiling technologies offer exciting possibilities for mapping the dynamic molecular changes underlying HSPC differentiation. Here, we have used single-cell RNA sequencing to profile more than 1600 single HSPCs, and deep sequencing has enabled detection of an average of 6558 protein-coding g  ...[more]

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