|
Status |
Public on Oct 10, 2020 |
Title |
04-NAP1KD2 |
Sample type |
SRA |
|
|
Source name |
S2_NAP1KD
|
Organism |
Drosophila melanogaster |
Characteristics |
cell line: S2 genotype/variation: NAP-1 knockdown
|
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 |
04-NAP1KD2_S4_L001
|
Data processing |
Basecalls performed using Illumina MiSeq RNA-seq reads were aligned to the Drosophila dm3 genome assembly using Illumina MiSeq Genome_build: Drosophila dm3 Supplementary_files_format_and_content: RPKM
|
|
|
Submission date |
Oct 09, 2020 |
Last update date |
Oct 10, 2020 |
Contact name |
Mitsuhiro Yoneda |
E-mail(s) |
yonedam@nagasaki-u.ac.jp
|
Phone |
81-95-819-7038
|
Organization name |
Nagasaki University
|
Street address |
1-12-4 Sakamoto
|
City |
Nagasaki |
ZIP/Postal code |
8528523 |
Country |
Japan |
|
|
Platform ID |
GPL16479 |
Series (1) |
GSE159294 |
Nucleosome assembly protein-1 (NAP-1) is regulator of histone H1 acetylation |
|
Relations |
BioSample |
SAMN16403297 |
SRA |
SRX9269759 |