|
Status |
Public on Jan 04, 2021 |
Title |
CTR_2 |
Sample type |
SRA |
|
|
Source name |
BMDC
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 tissue: bone marrow cell type: bone-marrow derived DC (BMDC) genotype: wildtype treatment: no treatment
|
Treatment protocol |
BMDCs were untreated or treated with either normal cell-derived exosomes or tumor cell-derived exosome for 24 hours
|
Growth protocol |
BMDCs were obtained by differentiating bone marrow cells with 20 ng/ml GM-CSF for 6 days
|
Extracted molecule |
total RNA |
Extraction protocol |
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 NovaSeq 6000 |
|
|
Data processing |
Illumina Casava1.7 software used for basecalling. The RNA-Seq raw data were processed through the standard RNA-Seq analysis pipeline. Briefly, read alignment was examined using TopHat2 version 2.1.1. Differential-expression analysis was carried out with DESeq2 version 1.24.0 in R v.3.3.1 (http://cran.r-project.org/). Genes were considered to be differentially expressed if the adjusted P was less than 0.05. Supplementary_files_format_and_content: raw counts
|
|
|
Submission date |
Aug 07, 2020 |
Last update date |
Jan 04, 2021 |
Contact name |
Wenfeng Zeng |
E-mail(s) |
zengwenfeng@ibp.ac.cn
|
Organization name |
Institute of Biophysics, Chinese Academy of Sciences
|
Street address |
15 Datun Road
|
City |
Beijing |
ZIP/Postal code |
100101 |
Country |
China |
|
|
Platform ID |
GPL24247 |
Series (1) |
GSE155881 |
Next Generation Sequencing Facilitates Quantitative Analysis of Transcriptomes of BMDCs treated without or with exosomes from tumor cells or normal cells |
|
Relations |
BioSample |
SAMN15760007 |
SRA |
SRX8909964 |