|
|
GEO help: Mouse over screen elements for information. |
|
Status |
Public on Apr 07, 2020 |
Title |
C8 |
Sample type |
SRA |
|
|
Source name |
Skin
|
Organism |
Heterocephalus glaber |
Characteristics |
tissue: Skin age (weeks): 43.33333333 individual id: F046
|
Extracted molecule |
genomic DNA |
Extraction protocol |
DNA was extracted from tissues using the PureLink™ Genomic DNA kit (Thermo Fisher, Cat. K182002), as per the manufacturer’s instructions. Tissues were digested overnight at 55 °C using 180 µl PK buffer and 20 µl PK enzyme from the kit. DNA concentration was quantified using a High Sensitivity DNA Qubit® assay (Life Technologies, Cat. Q32851). DNA from tissues was diluted to a concentration of 11 ng/µl and 45 µl of each sample was used for generation of targeted bisulfite sequencing data by the Genome Centre Facility at the Blizard Institute, Queen Mary University of London. DNA was bisulfite converted in a 96 well plate format using the EZ-96 DNA Methylation™ Kit (Zymo, Cat. D5003). Target amplification was performed using the FastStart High Fidelity PCR System, dNTPack (Sigma-Aldrich, Cat. 4738284001) in the 48.48 layout on the Fluidigm® C1 system (Fluidigm®, USA), a microfluidics platform. Library preparation was performed using the same kit including 4 μl of Access Array Barcode Library Primer and 1 μl of PCR product diluted 1:100. Libraries were sequenced with Illumina MiSeq sequencing using v2 chemistry (150 bp, paired-end).
|
|
|
Library strategy |
Bisulfite-Seq |
Library source |
genomic |
Library selection |
RANDOM |
Instrument model |
Illumina MiSeq |
|
|
Description |
BisPCRSeq_methylation_levels.csv
|
Data processing |
Raw FASTQ files were mapped to the reference hetGla2 using BISMARK (v0.16.3) and Bowtie2 (v2.2.8). Reads that mapped outside of the targeted regions were discarded from analyses, and methylated and unmethylated counts for each CpG were calculated using the custom C++ program (https://bitbucket.org/lowelabq- mul/methylation-extractor). Those CpGs with a coverage < 50× were also discarded from analyses Genome_build: hetGla2 Supplementary_files_format_and_content: csv file containing the fractional methylation level at each contig and position within included aDMP primers for each sample.
|
|
|
Submission date |
Sep 24, 2019 |
Last update date |
Apr 07, 2020 |
Contact name |
Amy Frances Danson |
E-mail(s) |
a.f.danson@qmul.ac.uk
|
Organization name |
The Blizard Institute
|
Department |
Centre for Genomics and Child Health
|
Lab |
Rakyan Lab
|
Street address |
2 Newark St
|
City |
London |
State/province |
Greater London |
ZIP/Postal code |
E1 2AT |
Country |
United Kingdom |
|
|
Platform ID |
GPL27526 |
Series (1) |
GSE137957 |
DNA methylation clocks as a predictor for ageing and age estimation in naked mole-rats, Heterocephalus glaber |
|
Relations |
BioSample |
SAMN12837164 |
SRA |
SRX6902301 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
|
|
|
|
|