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Status |
Public on Jul 03, 2024 |
Title |
NC_2 |
Sample type |
SRA |
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Source name |
Floral organ
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Organism |
Prunus sibirica |
Characteristics |
cultiva: Prunus sibirica clone tissue: Floral organ group: weak frost resistance clone developmental stage: Blooming stage
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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
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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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.
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Submission date |
Jul 20, 2021 |
Last update date |
Jul 03, 2024 |
Contact name |
Shengjun Dong |
E-mail(s) |
1996500037@syau.edu.cn
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Phone |
13898127077
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Organization name |
Shenyang Agricultural University
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Street address |
No.120 Dongling Road, Shenhe District, Shenyang, Liaoning Province, P.R.China.
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City |
Shenyang |
ZIP/Postal code |
110866 |
Country |
China |
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Platform ID |
GPL30412 |
Series (1) |
GSE180451 |
Transcriptomic analysis revealed genes involved in response to cold stress in Prunus sibirica |
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Relations |
BioSample |
SAMN20326023 |
SRA |
SRX11504297 |
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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