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Sample GSM6480818 Query DataSets for GSM6480818
Status Public on Jan 05, 2023
Title foxo_Sox15_mCherry_10-12_BS2
Sample type SRA
 
Source name embryos
Organism Drosophila melanogaster
Characteristics tissue: embryos
treatment: shmCherry (Control for foxo, Sox15)
timepoint: 10-12 hours
Extracted molecule polyA RNA
Extraction protocol Frozen embryos were homogenized using the Pellet Pestle Cordless Motor (Kimble Cat. No. 749540-0000; Pellet Pestles Sigma Cat. No. Z359947). RNA was extracted from the homogenate using TRIzol Reagent (Thermo Fisher, Cat. No. 15596026), chloroform extraction and isopropanol precipitation. RNA was resuspended in Nuclease Free Water (Ambion AM9930) and incubated over night before purification using the RNeasy Mini Kit (QIAGEN Cat. No. 74106). After Qiagen clean up, RNA was quantified using NanoDrop ND1000v 3.5.2.
Libraries for sequencing were made using TruSeq Stranded mRNA Library Prep (llumina 20020594).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Description Drosophila embryos RNAi, shmCherry (Control for foxo, Sox15), replicate 2, 10-12 hours
Data processing Raw FASTQ files were aligned to the Drosophila melanogaster reference genome (Release 6) using STAR aligner 2.7.3a with default settings and up to 20 multiple alignments to produce BAM files.
HTSeq htseq-count v0.12.4 was used to determine read counts overlapping genes.
Differential gene expression in the RNAi experimental samples compared to the mCherry controls was determined using DESeq2 1.24.0.
bigWig files were created using a custom tool called bam2bedgraph to convert bam files into bedgraph files, then UCSC's bedGraphToBigWig to convert the bedgraph files to bigWig format.
Assembly: dm6
Supplementary files format and content: BAM alignment files aligning FASTQ read files to dm6 assembly using STAR 2.7.3a.
Supplementary files format and content: HTSeq htseq-count files produced with HTSeq v0.12.4
Supplementary files format and content: DESeq csv files produced using DESeq2 v1.24.0
Supplementary files format and content: bigWig files produced using custom bam2bedgraph script and UCSC bedGraphToBigWig tool
 
Submission date Aug 18, 2022
Last update date Jan 06, 2023
Contact name Benjamin Wendell Booth
E-mail(s) [email protected]
Organization name Lawrence Berkeley National Laboratory
Department BioSciences
Lab Celniker
Street address 1 Cyclotron Road
City Berkeley
State/province CA
ZIP/Postal code 94720
Country USA
 
Platform ID GPL19132
Series (1)
GSE211573 A modERN Resource: Identification of Drosophila Transcription Factor candidate target genes using RNAi
Relations
BioSample SAMN30392821
SRA SRX17138095

Supplementary file Size Download File type/resource
GSM6480818_BS2_foxo_Sox15_mCherry_10-12.+.bw 55.5 Mb (ftp)(http) BW
GSM6480818_BS2_foxo_Sox15_mCherry_10-12.-.bw 56.7 Mb (ftp)(http) BW
GSM6480818_BS2_foxo_Sox15_mCherry_10-12.bw 106.6 Mb (ftp)(http) BW
GSM6480818_BS2_foxo_Sox15_mCherry_10-12.htseq-count.txt.gz 80.9 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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