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Status |
Public on May 01, 2021 |
Title |
J_R_0h_rep1 |
Sample type |
SRA |
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Source name |
root
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Organism |
Glycine max |
Characteristics |
tissue: root genotype: Wild type treatment: untreated
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Extracted molecule |
total RNA |
Extraction protocol |
TRIzol reagent method (Invitrogen) 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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Description |
JACK, untreated
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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.
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Submission date |
Apr 30, 2021 |
Last update date |
May 02, 2021 |
Contact name |
Wei Wei |
E-mail(s) |
[email protected]
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Phone |
8610-64807602
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Organization name |
Institute of Genetics and Developmental Biology
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Street address |
Chaoyang District, Beichen West Road, Campus #1, No 2
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City |
Beijing |
State/province |
Beijing |
ZIP/Postal code |
100101 |
Country |
China |
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Platform ID |
GPL28801 |
Series (1) |
GSE173640 |
Next Generation Sequencing Quantitative Analysis of soybean seeds Transcriptomes |
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Relations |
BioSample |
SAMN18929622 |
SRA |
SRX10722218 |
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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