|
Status |
Public on Apr 02, 2021 |
Title |
34 rep2 |
Sample type |
SRA |
|
|
Source name |
soybean
|
Organism |
Glycine max |
Characteristics |
genotype: Transgenic soybean (GmZF351) tissue: seed Stage: H3
|
Extracted molecule |
total RNA |
Extraction protocol |
TRIzol reagent method (Invitrogen) 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 |
RNA-sequencing was performed using an Illumina instrument of NovaSeq 6000 Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to Glycine max whole genome using Hisat2 Reads counting was performed using featureCounts software. Differential expressed genes were analyzed using DESeq2 software. Genome_build: Gmax_508_Wm82.a4.v1.gene.gtf Supplementary_files_format_and_content: counts.txt
|
|
|
Submission date |
Apr 01, 2021 |
Last update date |
Apr 02, 2021 |
Contact name |
Wei Wei |
Organization name |
Institute of Genetics and Developmental Biology, Chinese Academy of Sciences
|
Department |
State Key Lab of Plant Genomics
|
Street address |
Chaoyang District, Beichen West Road, Campus #1, No.2
|
City |
Beijing |
ZIP/Postal code |
100101 |
Country |
China |
|
|
Platform ID |
GPL28801 |
Series (1) |
GSE171304 |
Next Generation Sequencing Quantitative Analysis of soybean seeds Transcriptomes |
|
Relations |
BioSample |
SAMN18588815 |
SRA |
SRX10498533 |