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SRX850025: GSM1589294: CCE.4_13; Mus musculus; Bisulfite-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 1.9M spots, 339.7M bases, 192.4Mb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Single-cell DNA methylome sequencing and bioinformatic inference of epigenetic cell state dynamics
show Abstracthide Abstract
Here we describe a method for whole genome bisulfite sequencing in very small cell populations (µWGBS) and in single cells (scWGBS). Our method is optimized for profiling DNA methylation in many samples at low coverage, and we developed a bioinformatic method that uses collections of single-cell methylomes to infer cell state dynamics. Using these technological advances, we studied epigenetic cell state dynamics in three in vitro models of cellular differentiation and pluripotency and identified patterns of epigenetic remodeling and cell-to-cell heterogeneity. Overall design: 1-cell or 4-cell samples were collected from a variety of human and mouse cell lines (KBM7, CCE, K562, 32D, HL60). We also included negative controls (no cells), and cross controls (cells of one species aligned to the other). K562 cells were treated with 5-azacytidine in a final concentration of 1µM to induce demethylation. HL60 cells were treated with 1a,25-dihydroxyvitamin D3 in a final concentration of 10nM to induce differentiation. Naïve pluripotency of CCE ES cells was induced by culturing the cells in ESGRO-2i medium with the addition of 1% FCS. Differentiation of CCE ES cells was induced by treating the cells with all-trans retinoic acid (ATRA) in a final concentration of 0,3µM every third day along with complete LIF-free medium exchange. Embryoid body formation from CCE ES cells was induced by hanging-drop culture for 5 days, followed by 9 days on gelatinized dishes (see treatment annotation). Each experiment, with treated and untreated cells, was performed in multiple biological replicates. We then measured DNA methylation in the individual 1-cell or 4-cell experiments with bisulfite treatment and high-throughput sequencing. For sequencing, most experiments pooled a 4-cell experiment from one species with a 1-cell experiment from the other, but some replicates were sequenced as a single cell (indicated with SC in the replicate annotation). Two samples (marked as “deep”) were sequenced much deeper than the others. See Farlik et al. (2015) Cell Reports for complete study details.
Sample: CCE.4_13
SAMN03291047 • SRS824853 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina HiSeq 2000
Strategy: Bisulfite-Seq
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Direct extraction of DNA following the steps of the EZ DNA methylation Direct Kit as described in the methods section in Farlik et al. A novel method to perform library preparation from single cells as described in the methods section of Farlik et al.
Experiment attributes:
GEO Accession: GSM1589294
Links:
External link:
Runs: 1 run, 1.9M spots, 339.7M bases, 192.4Mb
Run# of Spots# of BasesSizePublished
SRR17691701,940,016339.7M192.4Mb2015-02-26

ID:
1199889

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