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SRX3697609: GSM3003535: Arabidopsis_Li_K; Arabidopsis thaliana; OTHER
2 ILLUMINA (Illumina HiSeq 2500) runs: 160.3M spots, 48.4G bases, 23.2Gb downloads

Submitted by: NCBI (GEO)
Study: Whole genome mapping of DNA G-quadruplexes in multiple species by G4-seq
show Abstracthide Abstract
The identification of DNA G-quadruplexes (G4s) in the genome is important to study different biological processes in which these structures play a role, such as genome rearrangement, transcriptional regulation and DNA replication. G4-seq allowed the high-throughput experimental mapping of G-quadruplexes in the human genome. We developed here an improved version of this method, named G4-seq2, which we applied to generate G-quadruplexes genomic maps for 12 species, selected as important models organism to study development or as pathogens of clinical relevance. Those multi-species maps, publicly available for the community, will allow to further understand the design principle of G-quadruplex formation in genomic context, to study G-quadruplex biology in those model organisms, to predict ligand targeting for therapeutic usage and to design G-quadruplex computational predictors based on genome-wide experimental measurements. Overall design: 24 library samples, 150 base pairs custom protocol (G4-Seq2) sequenced as two-times single-end reads on HiSeq 2500: 12 samples from different species for Li+ (Read-1) and K+ (Read-2); 12 samples from different species for Li+ (Read-1) and PDS+K+ (Read-2).
Sample: Arabidopsis_Li_K
SAMN08533580 • SRS2957109 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: OTHER
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: DNA was extracted with standard phenol/chloroform extraction as previously described in Chambers et. al 2015 (doi: 10.1038/nbt.3295), except for samples where DNA was purchased from companies (see source and characteristics field). Genomic DNA samples were sonicated and the library prepared, as in Chambers et al. 2015 (doi: 10.1038/nbt.3295). Libraries were prepared using the TruSeq Nano DNA LT Library Prep Kit (Nano in each sample file name), or with PCR-Free Library Prep Kit (PCRFree or not specified in each sample file name).
Experiment attributes:
GEO Accession: GSM3003535
Links:
Runs: 2 runs, 160.3M spots, 48.4G bases, 23.2Gb
Run# of Spots# of BasesSizePublished
SRR6724283102,696,58931G15.1Gb2018-08-02
SRR672428457,588,99617.4G8Gb2018-08-02

ID:
5104921

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