NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2813919 Query DataSets for GSM2813919
Status Public on Jun 30, 2018
Title (-) mild IMG1980 [21-P22]
Sample type SRA
 
Source name cultivar Rutgers
Organism Solanum lycopersicum
Characteristics genotype: msh1 memory line
background cultivar: Rutgers
tissue: leaf
Treatment protocol The top three leaves from each tomato plant (four weeks old) were collected and freeze in liquid nitrogen immediately and put into -80 ℃
Growth protocol Wild-type tomato (Solanum lycopersicum, cultivar Rutgers) and the corresponding, MSH1-RNAi segregate out (msh1 memory line) were germinated on MetroMix 200 medium (SunGro) and maintained at 26°C to 28°C with a 15-h day length and at 20°C to 22.8°C with a 9-h dark period.
Extracted molecule genomic DNA
Extraction protocol genomic DNA extraction using DNeasy Plant kit (Qiagen, Germany). Genomic DNA from three individual plants for both WT and msh1 memory line were used for subsequent Bisulfite methylome sequencing experiment.
Genomic DNA Sonicated to 100-300 bp fragments and purified with MiniElute PCR Purification Kit (Qiagen, Germany), incubated at 20 ℃ after add End Repair Mix. Then purified and added a single ‘A’ nucleotide to the 3’ ends of the blunt fragments, purified again and add Methylated Adapter to the 5’ and 3’ ends of each fragment. Then fragments with 300bp-400bp size-range were purified with QIAquick Gel Extraction kit (Qiagen, Germany) and subjected to bisulfite treatment by using Methylation-Gold kit (ZYMO). Followed with PCR and gel purification (350bp-400bp range fragments were selected). Qualified libraries sequenced pair end on the HiSeq X-ten system.
 
Library strategy Bisulfite-Seq
Library source genomic
Library selection RANDOM
Instrument model HiSeq X Ten
 
Description 21-P22
Data processing Illumina for basecalling
The sequences were trimmed using trim_galore 0.4.1 and cutadapt 1.9.1 with cutoff 20
The sequences were aligned using Erne-meth 2.1.1 with default options and set the output as a bismark coverage file
tab-delimited file generated with bismark2bedGraph with options -CX --ample_memory 
Genome_build: SL250 - Solanum_lycopersicum.SL2.50
Supplementary_files_format_and_content: tab-delimited file, 1-based genomic coords with <chromosome>  <start position>  <end position>  <methylation percentage>  <count methylated>  <count non-methylated> fields
 
Submission date Oct 16, 2017
Last update date May 15, 2019
Contact name Sally A Mackenzie
E-mail(s) sam795@psu.edu
Phone 814-863-8324
Organization name Penn State University
Department Biology
Lab Mackenzie
Street address 362 North Frear
City State College
State/province PA
ZIP/Postal code 16803
Country USA
 
Platform ID GPL24124
Series (1)
GSE105008 Bisulfite methylome sequencing of msh1 memory line in tomato
Relations
BioSample SAMN07788255
SRA SRX3287349

Supplementary file Size Download File type/resource
GSM2813919_21-P22.results.gz.bismark.cov.txt.gz 131.5 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap