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Sample GSM2193136 Query DataSets for GSM2193136
Status Public on Feb 11, 2017
Title TBD-623
Sample type SRA
 
Source name Peach
Organism Prunus persica
Characteristics cultivar: Troubador
development: Sampling at 35, 55, 75, 90, 105 days after full bloom
tissue: Fruit
flesh color: Yellow flesh
Treatment protocol Collect fruit at 35, 55, 75, 90, 105 days after full bloom,respectively
Growth protocol Six-year old ‘Troubador’ peach trees grown under standard field conditions at the National Peach Germplasm Repository in Nanjing, China.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from the fruit samples using Trizol reagent and subsequently treated with DNaseI (Takara Biotechnology Co., Ltd, Dalian, China) per the manufacturer’s instructions to remove contamination by genomic DNA.
sRNA fractions of 18 to 30 nt in length were first purified from the low-molecular weight RNA by excision from 15% denaturing polyacrylamide gels and then ligated to 3’ and 5’ adaptors using T4 RNA ligase according to the manufacturer’s instructions. The sRNAs ligated with 3’ and 5’ adaptors were purified and reverse transcribed to cDNA with the reverse transcription primers for 17 cycles according to the protocol. Eventually, the PCR products were further purified and subjected to sequencing using the Illumina Genome Analyzer. The image files obtained from the analyzer were then evaluated and used to form a large repertoire of digital data suitable for bioinformatics analysis. Degradome library was constructed following with methods previously described by Ma et al.(2010). CleaveLand3.0 program was used to detect potentially sliced targets of known and novel miRNA.
 
Library strategy miRNA-Seq
Library source transcriptomic
Library selection size fractionation
Instrument model Illumina HiSeq 2500
 
Data processing Raw sequencing reads were obtained using Illumina’s Pipeline v1.5 software
Sequencing image was analyzed by Pipeline Firecrest Module.
Base-calling was done by Pipeline Bustard Module
CleaveLand3.0 was used for alignment, filtering, peak-calling and so on.
Genome_build: http://www.ncbi.nlm.nih.gov/genome/388?genome_assembly_id=28754:assembly Prupe1_0
Supplementary_files_format_and_content: Profiles of Peach miRNAs.xls, miRNA sequence and expression data, Degradome_Targets_prediction.xlsx, miRNA target prediction results,target position and degradome fragments abundance on cleavage position
 
Submission date Jun 08, 2016
Last update date May 15, 2019
Contact name ZHANG chunhua
E-mail(s) [email protected]
Organization name Jiangsu Academy of Agricultural Sciences
Street address Xuanwu road
City Nanjing
ZIP/Postal code 210014
Country China
 
Platform ID GPL21993
Series (1)
GSE83110 The identification of known and novel microRNAs and their targets in peach (Prunus persica) fruit by high-throughput sequencing
Relations
BioSample SAMN05214399
SRA SRX1830195

Supplementary file Size Download File type/resource
GSM2193136_Summary_of_miRNAs.xlsx 37.2 Kb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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