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SRX5771225: GSM3741408: Chick_B2_smartseq2_scRNA-seq; Gallus gallus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 2.3M spots, 349.9M bases, 130.8Mb downloads

Submitted by: NCBI (GEO)
Study: Reconstruction of the global neural crest gene regulatory network in vivo [RNA-seq]
show Abstracthide Abstract
Precise control of developmental processes is encoded in the genome in the form of gene regulatory networks (GRNs). Such multi-factorial systems are difficult to decode in vertebrates owing to their complex gene hierarchies and transient dynamic molecular interactions. Here we present a genome-wide in vivo reconstruction of the GRN underlying development of neural crest (NC), an emblematic embryonic multipotent cell population. By coupling NC-specific epigenomic and single-cell transcriptome profiling with genome/epigenome engineering in vivo, we identify multiple regulatory layers governing NC ontogeny, including NC-specific enhancers and super-enhancers, novel trans-factors and cis-signatures. Assembling the NC regulome has allowed the comprehensive reverse engineering of the NC-GRN at unprecedented resolution. Furthermore, identification and dissection of divergent upstream combinatorial regulatory codes has afforded new insights into opposing gene circuits t hat define canonical and neural NC fates. Our integrated approach, allowing dissection of cell-type-specific regulatory circuits in vivo, has broad implications for GRN discovery and investigation. Overall design: Genome-wide transcriptome profiling avian neural crest (NC) at 2 different stages of the NC ontogeny isolted from their in vivo context.
Sample: Chick_B2_smartseq2_scRNA-seq
SAMN11539110 • SRS4705112 • All experiments • All runs
Organism: Gallus gallus
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Individual NC cells were collected by FACS, cDNA was generated and sequencing libraries were prepared as previously described (Picelli, Faridani et al. 2014). Libraries were sequenced using 50bp single-end reads for 96 cells on the Illumina NextSeq500 platform. A 4x107 dilution of ERCC spike in control was used. SMARTseq2
Links:
Runs: 1 run, 2.3M spots, 349.9M bases, 130.8Mb
Run# of Spots# of BasesSizePublished
SRR89921722,257,821349.9M130.8Mb2019-10-10

ID:
7761072

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