|
Status |
Public on Jun 15, 2023 |
Title |
2-4h embryo Control Rep4 |
Sample type |
SRA |
|
|
Source name |
Whole embryo
|
Organism |
Drosophila melanogaster |
Characteristics |
tissue: Whole embryo genotype: tub-GAL4/+ developmental stage: 2-4h after egg laying treatment: Control
|
Growth protocol |
Embryos were grown at 25°C
|
Extracted molecule |
total RNA |
Extraction protocol |
Embryos were homogenized in 300 µL TRIzol LS Reagent followed by total RNA purification using the Direct-zol RNA MiniPrep kit (R2050, ZymoResearch). RNA libraries were prepared using the TruSeq Stranded Total RNA kit (Illumina).
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Data processing |
usegalaxy.eu RNA-seq reads were mapped to the Drosophila melanogaster (dm6) genome assembly using STAR with default parameters. RNA-seq count tables were generated with featureCounts and differential expression analysis (DE) of HDAC3 shRNA vs. Control, shRNA-resistant rescueWT, shRNA-resistant rescueY303F, shRNA-resistant rescueK26A or shRNA-resistant rescueHEBI was performed using DEseq2. Assembly: dm6 Supplementary files format and content: xlsx file for RNA-seq count table
|
|
|
Submission date |
Jun 16, 2022 |
Last update date |
Jun 15, 2023 |
Contact name |
Mattias Mannervik |
E-mail(s) |
mattias.mannervik@su.se
|
Organization name |
Stockholm University
|
Street address |
Svante Arrhenius väg 20C
|
City |
Stockholm |
ZIP/Postal code |
10691 |
Country |
Sweden |
|
|
Platform ID |
GPL19132 |
Series (2) |
GSE206247 |
Separation of transcriptional repressor and activator functions in HDAC3 [RNA-Seq] |
GSE206249 |
Separation of transcriptional repressor and activator functions in HDAC3 |
|
Relations |
BioSample |
SAMN29135691 |
SRA |
SRX15720269 |