|
Status |
Public on Jan 13, 2016 |
Title |
control for experiment with highly downregulated Satb1, replicate 2 |
Sample type |
SRA |
|
|
Source name |
WT_tumor-associated DC
|
Organism |
Mus musculus |
Characteristics |
strain background: C57BL/6 genotype/variation: bearing ID8-Defb29/Vegf-a treated with: Non-Targeting (NT) siRNA satb1 status: wildtype cell type: Cancer-Associated Dendritic Cells (DCs) replicate: 2
|
Treatment protocol |
mice (C57BL/6) were treated for 32-38 days with 100 μg of Non-Targeting (NT) or Satb1 siRNA-Rhodamine conjugated polyethylenimine nanocomplexes (Satb1)
|
Growth protocol |
mice (C57BL/6) bearing ID8-Defb29/Vegf-a grown for 32-38 days
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated for RNA-Seq using Trizol reagent. RNA-Seq library was prepared using the TruSeq Stranded Total RNA Library Preparation kit (Illumina).
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
endogenous level of Satb1 high.NT.2
|
Data processing |
RNA-Seq data analyzing was done with rsem(ver. 1.2.12) and mm9 genome with UCSC known gene set. DESeq2 was used for differentail expression analysis Genome_build: mm9 Supplementary_files_format_and_content: FPKM and raw count values for all UCSC genes across 6 samples
|
|
|
Submission date |
Jan 12, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Priyankara J Wickramasinghe |
E-mail(s) |
priyaw@wistar.org
|
Phone |
2154956837
|
Organization name |
The Wistar Institute
|
Department |
Bioinformatics
|
Lab |
Genomics
|
Street address |
3601 Spruce Street
|
City |
Philadelphia |
State/province |
PA |
ZIP/Postal code |
19104 |
Country |
USA |
|
|
Platform ID |
GPL13112 |
Series (1) |
GSE76776 |
Satb1 Overexpression Drives Tumor-Promoting Activities In Cancer-Associated Dendritic Cells |
|
Relations |
BioSample |
SAMN04397439 |
SRA |
SRX1528500 |