|
Status |
Public on Jul 14, 2022 |
Title |
20d_rep_2 |
Sample type |
SRA |
|
|
Source name |
Red blood cell in rat
|
Organism |
Rattus norvegicus |
Characteristics |
treatment: stored 20-day periods with citrate–phosphate–dextrose solution with adenine (CPDA) at 4°C cell type: Red blood cells age: 11 weeks genotype: Wild type
|
Treatment protocol |
The following 3 experimental conditions were set for rat whole blood depending storage periods: Control (Cont; no storage), 10 days (10d), and 20 days (20d) group.
|
Growth protocol |
Standard protocol
|
Extracted molecule |
total RNA |
Extraction protocol |
RNAs were extracted from the purified RBC, using RNAiso Blood (Cat#9112; Takara Bio) Libraries were constructed using NEBNext Ultra II RNA Library Prep Kit for Illumina, and NEBNext rRNA Depletion Kit (Cat# E7770 and E6310; New England Biolabs).
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Data processing |
The RNA-Seq reads were aligned to the mRatBN7.2 genome assembly using CLC genomics workbench 22.0 with the default settings. A statistical differential expression test was used "Differential Expression for RNA-Seq tool" in the CLC software. Supplementary files format and content: Excel file of statistic test and expression data.
|
|
|
Submission date |
Jun 10, 2022 |
Last update date |
Jul 14, 2022 |
Contact name |
takehito sugasawa |
E-mail(s) |
[email protected]
|
Phone |
+81-29-853-3209
|
Organization name |
University of tsukuba
|
Street address |
Ibaraki
|
City |
Tsukuba |
State/province |
Select State |
ZIP/Postal code |
3058577 |
Country |
Japan |
|
|
Platform ID |
GPL20084 |
Series (1) |
GSE205806 |
Identification of RNA Markers in Red Blood Cells for Doping Control in Autologous Blood Transfusion |
|
Relations |
BioSample |
SAMN28956620 |
SRA |
SRX15663427 |