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Sample GSM5462975 Query DataSets for GSM5462975
Status Public on Jul 03, 2024
Title NC_2
Sample type SRA
 
Source name Floral organ
Organism Prunus sibirica
Characteristics cultiva: Prunus sibirica clone
tissue: Floral organ
group: weak frost resistance clone
developmental stage: Blooming stage
Extracted molecule total RNA
Extraction protocol Select the natural frost-damaged Prunus sibirica flower organs, use the kit method to extract RNA, and use the Illumina sequencing platform to construct a sequencing library to extract RNA
The six RNA libraries were prepared for sequencing using standard Illumina protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing The sequencing-obtained raw image data were converted to sequence reads using CASAVA.
The raw data was filtered by R language, and finally the clean reads for subsequent analysis were obtained.
Trinity v2.4.0 program was used to stitch and assemble clean reads of all samples. Redundancy was removed by clustering with Corset hierarchy, The longest transcript of each gene was selected as Unigene for subsequent analysis.
The transcript sequence obtained by splicing with Trinity was used as a reference sequence. RSEM software (version v1.2.15) (bowtie2, mismatch=0) (bowtie2 default parameters, mismatch = 0)was used to compare clean reads of each repeated sample with reference sequences, and the readcount of each gene was counted and compared. FPKM (fragments per kilobase of exon per million mapped fragments) was used to standardize the readcount of genes.
The DEGseq R package (1.12.0) was used for differential expression analyses. The P-value was calculated based on a negative binomial distribution model. P-values was adjusted using the Benjamini-Hochberg mothed (Benjamini and Hochberg, 1995). Genes with an adjusted P-value < 0.05 and log2(Fold change) > 1 were assigned as differentially expressed.
Genome_build: Prunus armeniaca
Supplementary_files_format_and_content: FPKM file includes gene ID and expression for each sample.
 
Submission date Jul 20, 2021
Last update date Jul 03, 2024
Contact name Shengjun Dong
E-mail(s) 1996500037@syau.edu.cn
Phone 13898127077
Organization name Shenyang Agricultural University
Street address No.120 Dongling Road, Shenhe District, Shenyang, Liaoning Province, P.R.China.
City Shenyang
ZIP/Postal code 110866
Country China
 
Platform ID GPL30412
Series (1)
GSE180451 Transcriptomic analysis revealed genes involved in response to cold stress in Prunus sibirica
Relations
BioSample SAMN20326023
SRA SRX11504297

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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