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SRX704166: GSM1507570: haematopoietic stem cell [HSC1_8]; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 1.9M spots, 387.2M bases, 225.2Mb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Molecular signatures of heterogeneous stem cell populations are resolved by linking single cell functional assays to single cell gene expression
show Abstracthide Abstract
The discovery of significant heterogeneity in the self-renewal durability of adult haematopoietic stem cells (HSCs) has challenged our understanding of the molecules involved in population maintenance throughout life. Gene expression studies in bulk populations are difficult to interpret since multiple HSC subtypes are present and HSC purity is typically less than 50% of the input cell population. Numerous groups have therefore turned to studying gene expression profiles of single HSCs, but again these studies are limited by the purity of the input fraction and an inability to directly ascribe a molecular program to a durable self-renewing HSC. Here we combine single cell functional assays with flow cytometric index sorting and single cell gene expression assays to gain the first insight into the gene expression program of HSCs that possess durable self-renewal. This approach can be used in other stem cell systems and sets the stage for linking key molecules with defined cellular functions. Overall design: single-cell RNA-Seq of haematopoietic stem cells
Sample: haematopoietic stem cell [HSC1_8]
SAMN03073696 • SRS703811 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Bone marrow cells were isolated from the bones (femurs and tibiae) of 9–12-week-old C57BL/6 mice. Cells were stained with antibodies to permit the separation of the individual populations. A FACS Influx (BD Biosciences) was used for all single-cell sorting, unstained populations and single-stains were used as gate-setting controls. Single cells were sorted by FACS directly into individual wells of a 96-well plate containing lysis buffer. Single cell RNA-Seq analysis was performed as described previously (Picelli et al., 2014). Pooled libraries were then run on the Illumina Hi-Seq 2500. single cell RNA libraries were prepared for sequencing using the Illumina Nextera XT DNA preparation kit
Experiment attributes:
GEO Accession: GSM1507570
Links:
External link:
Runs: 1 run, 1.9M spots, 387.2M bases, 225.2Mb
Run# of Spots# of BasesSizePublished
SRR15786501,935,761387.2M225.2Mb2015-05-26

ID:
992835

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