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SRX7064720: GSM4142197: T5.WGBS.AD; Trichinella murrelli; Bisulfite-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 14.2M spots, 4.3G bases, 1.5Gb downloads

Submitted by: NCBI (GEO)
Study: 12 single-base resolution methylomes of three life stages using WGBS
show Abstracthide Abstract
As the most studied type of epigenetic modifications found in many taxa, DNA methylation has been confirmed to play a crucial role in transposon silencing, transcriptional regulation and thus phenotypic variation, as well as rapid adaption to changing environments. To fully understand the methylome variation in Trichinella, here, we report 12 single-base resolution methylomes of three life stages using WGBS. By comparative epigenomics, we observe that the methylome variation in Trichinella is significantly divergent and host-related. By comparative epigenomics, we observe that the methylome variation in Trichinella is significantly divergent and host-related. By comparing DNA methylation patterns between different host classes of species, we found a fraction of parasitism-related genes under epigenetic regulation, such as G-protein-coupled receptor, DNaseII and ligand-gated chloride channel. Moreover, we also reveal associations between methylation divergence and genetic basis, including nucleotide variant and structural variation. Overall design: We report 12 single-base resolution methylomes of three life stages using WGBS
Sample: T5.WGBS.AD
SAMN13140921 • SRS5581285 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: Bisulfite-Seq
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: DNA was extracted using the phenol chloroform extraction method Genomic DNA extracted from three life stages of all Trichinella species were selected for libraries construction of WGBS. Briefly, approx. two to five micrograms of gDNA were first fragmented by Covaris to an average size of ~200-300 bp. End-repair, A-tailing and ligation were conducted as the Illumina PE genomic DNA sample prep kit protocol, except that ligation was performed using methylated cytosine PE adapters provided by Illumina previously. Ligation products were purified and bisulfited converted using the EZ DNA Methylation-Gold KitTM (ZYMO) according to the manufacturer's instructions. The libraries were sequenced using Illumina HiSeq 2,500 platform.
Experiment attributes:
GEO Accession: GSM4142197
Links:
Runs: 1 run, 14.2M spots, 4.3G bases, 1.5Gb
Run# of Spots# of BasesSizePublished
SRR1035511514,236,5854.3G1.5Gb2020-06-01

ID:
9289394

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