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Sample GSM2881082 Query DataSets for GSM2881082
Status Public on May 27, 2018
Title reseq_jizi
Sample type SRA
 
Source name young panicle
Organism Oryza sativa Japonica Group
Characteristics cultivar: JZ1560
tissue: young panicle
Growth protocol The rice seeds were germinated in sterilized water, and were then placed in soil in an experimental field of the Institute of Plant Physiology and Ecology (Shanghai, China) under natural growing conditions during kharif season of 2013. Panicles were harvested.
Extracted molecule genomic DNA
Extraction protocol Harvested samples were either frozen in liquid nitrogen for re-sequencing and RNA sequencing. or directly vacuum-infiltrated with formaldehyde cross-linking solution for ChIP assay. For rice samples, ChIP assay was performed with the antibody against H3 trimethyl-Lys 4 (Abcam, Cat. ab8580), H3 monomethyl-Lys 4 (Millipore,07-436), H3 trimethyl-Lys 27 (Upstate, USA, Cat. 07–449), H3 acetyl-Lys 27 (Upstate, USA, Cat. 07–360) and H3 trimethyl-Lys 36 (Abcam, Cat. ab9050)
Library construction and deep sequencing were performed by Genergy Biotechnology Co. Ltd. (Shanghai, China). Libraries were sequenced on the HiSeq 2500 (Illumina) to produce 51 bp single reads for rice ChIP-seq, and 101 bp paired reads for re-sequencing and RNA sequencing.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina HiSeq 2500
 
Description Re-Sequencing
Data processing The sequencing reads were cleaned, including removing bases with low quality score (<20) and irregular GC content based on FastQC, cutting sequencing adaptor followed by filtering short reads.
The cleaned reads were mapped to oryza sativa(MSU7.0) using bwa mem or tophat2 to map with default settings.
The duplicated reads were removed, and only alignments with MAPQ score > 20 were kept for further analysis.
For ChIP-seq, macs 1.3 was used to identify read enriched regions(peaks). For RNA-Seq, HTSeq-count was used to count the RNA-seq alignment files.
Genome_build: MSU 7.0
Supplementary_files_format_and_content: In ChIP-Seq, peak files was provided; In RNA-Seq, read counts for genes(MSU7.0) was provided.
 
Submission date Dec 07, 2017
Last update date May 27, 2018
Contact name yijing zhang
E-mail(s) zhangyijing@fudan.edu.cn
Organization name Fudan University
Department Biochemistry
Lab Functional Epigenomics Group
Street address 2005 Songhu Road
City shanghai
ZIP/Postal code 200438
Country China
 
Platform ID GPL18525
Series (1)
GSE107827 de novo re-construction of the core genome from ChIP-Seq for large-genome organisms
Relations
BioSample SAMN08146255
SRA SRX3455779

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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