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Series GSE117117 Query DataSets for GSE117117
Status Public on Sep 07, 2018
Title RNA-seq analysis comparing gene expression in Drosophila sea mutants and controls
Organism Drosophila melanogaster
Experiment type Expression profiling by high throughput sequencing
Summary The goal of this study was to determine how decreased mitochondrial citrate export influences gene expression in Drosophila larvae. RNA was isolated from Drosopohila sea mutants, which exhibiti decreased mitochondrial citrate transport activity, and a genetically-matched control strain during mid-L3 development.
 
Overall design Larvae were collected as described in Li, H., Tennessen, J. M. Preparation of Drosophila Larval Samples for Gas Chromatography-Mass Spectrometry (GC-MS)-based Metabolomics. J. Vis. Exp. (136), e57847, doi:10.3791/57847 (2018). RNA was purified from staged mid-L3 larvae using a RNeasy Mini Kit (Qiagen). Sequencing was performed using an Illumina NextSeq500 platform with 75 bp sequencing module generating 41 bp paired-end reads. After the sequencing run, demultiplexing was performed with bcl2fastq v2.20.0.422.
 
Contributor(s) Li H, Tennessen J
Citation(s) 30108060
Submission date Jul 13, 2018
Last update date Mar 22, 2019
Contact name Jason Tennessen
E-mail(s) jtenness@indiana.edu
Phone 812 855 9803
Organization name Indiana University
Department Department of Biology
Street address 1001 E. Third St
City Bloomington
State/province IN
ZIP/Postal code 47405
Country USA
 
Platforms (1)
GPL19132 Illumina NextSeq 500 (Drosophila melanogaster)
Samples (6)
GSM3271514 GSF1670_Tennessen_C1
GSM3271515 GSF1670_Tennessen_C2
GSM3271516 GSF1670_Tennessen_C3
Relations
BioProject PRJNA481071
SRA SRP153550

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE117117_RAW.tar 440.0 Kb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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