|
Status |
Public on Jul 25, 2024 |
Title |
2_WT_SAG |
Sample type |
SRA |
|
|
Source name |
primary MEF
|
Organism |
Mus musculus |
Characteristics |
cell type: primary MEF genotype: WT treatment: 100 nM SAG for 24 h
|
Extracted molecule |
total RNA |
Extraction protocol |
Total cellular RNA was extracted with using RNeasy mini kit (QIAGEN) with DNase I treatment (QIAGEN). stranded library preparation with polyA selection
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 1000 |
|
|
Data processing |
Cutadapt v1.9.1 was used to trim and filter reads, and clean data were aligned to the reference genome (ENSEMBLE, GRCm38.97) using the software HISAT 2 (v2.0.1). Assembly: ENSEMBL, GRCm38.97 Supplementary files format and content: Relative gene expression was quantified and normalized in a FPKM format
|
|
|
Submission date |
May 17, 2024 |
Last update date |
Jul 25, 2024 |
Contact name |
SAISHU YOSHIDA |
E-mail(s) |
saishu@hotmail.co.jp
|
Phone |
0474721158
|
Organization name |
Toho University
|
Department |
Department of Biomolecular Science,
|
Street address |
2-2-1 Miyama, Funabashi-shi
|
City |
Chiba |
ZIP/Postal code |
274-8510 |
Country |
Japan |
|
|
Platform ID |
GPL15103 |
Series (1) |
GSE267749 |
Positive regulation of Hedgehog signaling via phosphorylation of GLI2/GLI3 by DYRK2 kinase |
|
Relations |
BioSample |
SAMN41443071 |
SRA |
SRX24598600 |