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Sample GSM2249875 Query DataSets for GSM2249875
Status Public on Aug 31, 2017
Title OSS_146_RNA_siPIWI
Sample type SRA
 
Source name OSS_RNA_siPIWI
Organism Drosophila melanogaster
Characteristics cell line: OSS
cell type: ovarian follicle cell culture
sirna knockdown of: PIWI
rna extracted from: cytoplasm lysates
Treatment protocol For each experiment, 500 pmoles siRNAs were electroporated into a 10cm plate of OSS cells using Amaxa kit V (program D013), and cells were cultured for 6 days before harvesting.
Growth protocol OSS cells were cultured in a customly assembled media comprised of fly extract, M13 media, FBS, insulin, and glutathione. See the full protocol from Lau et al, Genome Res, 2009.
Extracted molecule total RNA
Extraction protocol Total RNA from NUN pellets or cytoplasm lysates were extracted with the Tri-reagent protocol of Chomzcynski and and Sacchi, 1987.
New Englad Bioloabs, NEBNext Ultra Directional RNA Library Prep Kit for Illumina.
Eight libraries with different barcodes were multiplexed in each sequencing run. Separation of sequences by different barcodes was conducted during the on-instrument base-calling.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Data processing Illumina Nextseq 500 on instrument base calling
FastX initial quality score trimming and filtering of reads against structural RNAs, microRNAs, viral RNAs
Mapped to the Drosophila melanogaster reference genome, build Dm3 / Release 5, with Bowtie, allowing up to 2 mismatches
For just the 146_NUN set (siGFP, siPIWI, siPAF1 and siPIWI+siPAF1), a "jackpot" reads filter was applied to remove any sequences whose read count was greater than 50 reads.
SAM file of reads counted against RefSeq database of all Drosophila transcripts, counts per locus region and both strands measured
Genome_build: Drosophila melanogaster genome build Release 5.1, Dm3
Supplementary_files_format_and_content: text file tab-delimited tables of read counts mapped to refseq transcripts
 
Submission date Jul 25, 2016
Last update date May 15, 2019
Contact name NELSON LAU
E-mail(s) nclau@bu.edu
Organization name Boston University School of Medicine
Department Biochemistry
Street address 72 E Concord St K219, Dept of Biochemistry
City BOSTON
State/province MA
ZIP/Postal code 02118
Country USA
 
Platform ID GPL19132
Series (1)
GSE84766 Paf1 modulates Piwi/piRNA silencing capacity in Drosophila
Relations
Reanalyzed by GSM3281706
BioSample SAMN05437374
SRA SRX1973486

Supplementary file Size Download File type/resource
GSM2249875_processed_OSS_146_RNA_siPIWI.fastq-50-0.02.txt.gz 1.0 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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