|
Status |
Public on Feb 05, 2018 |
Title |
SLE-peli1-low2 |
Sample type |
SRA |
|
|
Source name |
SLE-peli1-low_peripheral blood
|
Organism |
Homo sapiens |
Characteristics |
subject status: SLE patient peli1 expression level: low tissue: Peripheral blood
|
Extracted molecule |
total RNA |
Extraction protocol |
PBMCs were isolated from Peripheral blood,and RNA was harvested using Trizol reagent. RNA libraries were prepared for sequencing using standard Illumina protocols
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 4000 |
|
|
Data processing |
Transcriptomic reads from the RNA-Seq experiments were mapped to a reference genome (mm10) using Bowtie. Gene expression levels were quantified using the RSEM software package. Differentially expressed genes were subsequently analyzed using the DAVID bioinformatics platformand IPA. Genome_build: hg38 Supplementary_files_format_and_content: Processed data were txt format and all gene FPKM of each sample were contained in each txt file.
|
|
|
Submission date |
Jul 14, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Junli Liu |
E-mail(s) |
[email protected]
|
Organization name |
Institute of Health Sciences Shanghai Institutes for Biological Sciences Chinese Academy of Sciences
|
Street address |
New Research Buliding,320 Yue Yang Road Shanghai, P.R.China
|
City |
上海 |
ZIP/Postal code |
200031 |
Country |
China |
|
|
Platform ID |
GPL20301 |
Series (1) |
GSE101437 |
Next Generation Sequencing Facilitates Quantitative Analysis of Health donors and SLE patients' PBMC Transcriptomes |
|
Relations |
BioSample |
SAMN07350922 |
SRA |
SRX3005300 |