|
Status |
Public on Jul 01, 2024 |
Title |
L1_rep1 |
Sample type |
SRA |
|
|
Source name |
Whole worms
|
Organism |
Caenorhabditis elegans |
Characteristics |
tissue: Whole worms cell line: Bristol N2 cell type: hermaphrodite genotype: wild-type treatment: feeding L1
|
Treatment protocol |
Three-day-old worms were cultured for six hours on mNGM plates covered with OP50 (control group) or L. lactis.
|
Extracted molecule |
total RNA |
Extraction protocol |
Approximately 200 worms in each group were collected and soaked in RNAlater solution (Qiagen). Total RNA was isolated using the RNeasy Lipid Tissue kit (Qiagen). mRNAs were purified using the NEBNext Poly(A) mRNA Magnetic Isolation Module. Libraries were prepared using the SMARTerĀ® Stranded Total RNA-Seq Kit (Clontech)
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 4000 |
|
|
Data processing |
Illumina Real-Time Analysis (RTA) software used for basecalling. The raw reads were trimmed and quality-filtered using the Trim Galore! (ver. 0.6.6), Trimmomatic (ver. 0.39) and cutadapt (ver. 3.1) software. Clean reads were aligned versus the N2 Caenorhabditis elegans reference genome ce11 (WBcel235.104) using STAR (ver. 2.7.9a). The read count of gene features was performed with the featureCounts tool (ver. 2.0.1) Assembly: ce11 Supplementary files format and content: tab-delimited text files include featureCount values for each sample
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|
|
Submission date |
Mar 08, 2024 |
Last update date |
Jul 01, 2024 |
Contact name |
Eriko Kage-Nakadai |
E-mail(s) |
nakadai@omu.ac.jp
|
Organization name |
Osaka Metropolitan Univ.
|
Street address |
3-3-138, Sugimoto, Sumiyoshi-ku
|
City |
Osaka |
State/province |
Osaka |
ZIP/Postal code |
558-8585 |
Country |
Japan |
|
|
Platform ID |
GPL22765 |
Series (1) |
GSE261173 |
Characterization of the genes that were regulated by feeding Lactococcus Lactis. |
|
Relations |
BioSample |
SAMN40333691 |
SRA |
SRX23883899 |