|
Status |
Public on Jul 12, 2016 |
Title |
control-1 |
Sample type |
SRA |
|
|
Source name |
embryos
|
Organism |
Drosophila melanogaster |
Characteristics |
cell line: S2 genotype/variation: control
|
Growth protocol |
S2 cells were grown in Schneider’s Drosophila media (Gibco) with 10% FBS.
|
Extracted molecule |
total RNA |
Extraction protocol |
S2 cells were collected.Total RNA was isolated using ISOGEN II reagent (NIPPON GENE), according to the manufacturer’s protocol. RNA-seq libraries were prepared using the TruSeq Stranded mRNA LT Sample Prep kit (Illumina)
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina MiSeq |
|
|
Description |
Sample 1
|
Data processing |
Basecalls performed using Illumina MiSeq RNA-seq reads were aligned to the Release 5 (dm3) genome assembly using Illumina MiSeq Partek genomic suite was used to generate RPKMs. Quantification was performed using transcript-level and a significant signal was filtered by including at least one of the signal having more than one RPKM. Genome_build: Release 5 (dm3) Supplementary_files_format_and_content: RPKM
|
|
|
Submission date |
Sep 16, 2015 |
Last update date |
May 15, 2019 |
Contact name |
TAKEYA NAKAGAWA |
E-mail(s) |
takeyanoemail@gmail.com
|
Organization name |
Nagasaki unversity
|
Department |
Biochemistry
|
Street address |
1-12-4 sakamoto
|
City |
Nagasaki |
ZIP/Postal code |
852-8523 |
Country |
Japan |
|
|
Platform ID |
GPL16479 |
Series (1) |
GSE73098 |
Chameau Activates Transcription with Enhancer of Acetyltransferase Chameau (EAChm) in vitro |
|
Relations |
Reanalyzed by |
GSM3276731 |
BioSample |
SAMN04090373 |
SRA |
SRX1250572 |