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Status |
Public on Aug 15, 2017 |
Title |
seed following 48 h of stratification (S) Replicate 3 [methylC-seq] |
Sample type |
SRA |
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|
Source name |
seed following 48 h of stratification (S)
|
Organism |
Arabidopsis thaliana |
Characteristics |
ecotype: Col0 genotype/variation: wild type tissue: germinating seed time point: seed during stratification 48 h S
|
Treatment protocol |
Samples were collected 48 h into dark stratification started at 4 °C. Seed was collected freshly harvested (H), after 14 days of drying (0 h), 1, 12 and 48 h during stratification and 1, 6, 12, 24, 48 h in continuous light.
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Growth protocol |
Seeds were sown on MS media, statified at 4 C for 2-d before being transferred to continious light at 22C.
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Extracted molecule |
genomic DNA |
Extraction protocol |
gDNA was extracted from the seeds/seedlings using the Qiagen DNeasy Plant minikit and 600ng of purified gDNA was used for MethylC-seq library preparation after spiking in 0.5% lambda DNA (N6-methyladenine-free) (New England BioLabs). MethylC-seq library preparation was carried out as described previously (Urich et al., 2015 - http://www.nature.com/nprot/journal/v10/n3/full/nprot.2014.114.html).
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Library strategy |
Bisulfite-Seq |
Library source |
genomic |
Library selection |
RANDOM |
Instrument model |
Illumina HiSeq 1000 |
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Description |
48hS_3
|
Data processing |
Sequenced reads were trimmed for adaptor sequence, and filtered for low-quality sequence, with Trim Galore v0.4.2 filered and trimmed reads were mapped with bismark v0.16.3 with default parameters Deduplicated reads (deduplicate_bismark) were used to generate genome-wide cytosine reports (bismark_methylation_extractor, bismark2bedGraph, coverage2cytosine) DMRs were identified using HOME (hten used to identify timeseries DMRs for three context CG, CHG and CHH using HOME-timeseries with default parameters. We further filtered out regions whose maximum absolute difference in methylation during the timecourse was lower than 20%. Genome_build: TAIR10 Supplementary_files_format_and_content: tab-delimited files including genome-wide cytosine report, and bed files of unfiltered DMRs in CG, CHG and CHH contexts.
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Submission date |
Feb 03, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Quentin Gouil |
Organization name |
Olivia Newton-John Cancer Research Institute
|
Lab |
Health and Epigenomics Across Life
|
Street address |
Studley Road
|
City |
Heidelberg |
State/province |
VIC |
ZIP/Postal code |
3085 |
Country |
Australia |
|
|
Platform ID |
GPL17311 |
Series (2) |
GSE94456 |
methylC-seq data over Arabidopsis thaliana germination |
GSE94459 |
methylC-seq, RNA-seq and sRNA-seq data over Arabidopsis thaliana germination |
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Relations |
BioSample |
SAMN06293564 |
SRA |
SRX2536470 |