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Status |
Public on May 27, 2018 |
Title |
reseq_jizi |
Sample type |
SRA |
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Source name |
young panicle
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Organism |
Oryza sativa Japonica Group |
Characteristics |
cultivar: JZ1560 tissue: young panicle
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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.
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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.
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Library strategy |
OTHER |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 2500 |
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Description |
Re-Sequencing
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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.
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Submission date |
Dec 07, 2017 |
Last update date |
May 27, 2018 |
Contact name |
yijing zhang |
E-mail(s) |
zhangyijing@fudan.edu.cn
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Organization name |
Fudan University
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Department |
Biochemistry
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Lab |
Functional Epigenomics Group
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Street address |
2005 Songhu Road
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City |
shanghai |
ZIP/Postal code |
200438 |
Country |
China |
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Platform ID |
GPL18525 |
Series (1) |
GSE107827 |
de novo re-construction of the core genome from ChIP-Seq for large-genome organisms |
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Relations |
BioSample |
SAMN08146255 |
SRA |
SRX3455779 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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