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Sample GSM1226165 Query DataSets for GSM1226165
Status Public on Dec 19, 2013
Title GM12878 native deproteinized replicate 1, S1
Sample type SRA
 
Source name rRNA depleted RNA S1 nuclease at 37°C
Organism Homo sapiens
Characteristics sample type: rRNA depleted
cell line: GM12878
Biomaterial provider Coriell; http://ccr.coriell.org/Sections/Search/Search.aspx?PgId=165&q=GM12878
Treatment protocol RNA is isolated from the cells using 1) Trizol and poly(A)+ selected or 2)lysed with 0.1% SDS, 0.25% Na deoxycholate, phenol extracted, before structure probing at 37˚C
Growth protocol GM12878, GM12891 and GM12892 cells were grown at 37˚C to ~0.6million cells/ml in RPMI media supplemented with 15% FBS, 2mM L-glutamine and 1% PenStep
Extracted molecule total RNA
Extraction protocol The cleavage sites are captured and cloned using Ambion RNA sequencing kit compatible with the Illumina platform (Ambion)
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description Single strand RNA structure probing and deep sequencing of double stranded regions in Human transcriptome GM12878
Data processing Raw reads were trimmed to 50bp (trimmed 51bp from the 3'end)
Trimmed reads were mapped to hg19 transcriptome using bowtie2, where the hg19 transcriptome was aggragated from UCSC RefSeq and Gencode v12 databases
The number of single and double strand reads were calculated by passing through the SAM file accordingly, and numbers were then normalized by sequencing depth
Genome_build: Hg19 Transcriptome, aggragated from UCSC RefSeq and Gencode v12 databases
Supplementary_files_format_and_content: The processed .tab file contains two tab-seprated columns, the first column is the transcript ID, and the second column is a list of semi-colon seprated numbers indicating the S1/V1 counts for each base of that transcript
Supplementary_files_format_and_content: On the Series record, a table of transcript-level normalized counts.
 
Submission date Sep 06, 2013
Last update date May 15, 2019
Contact name Kun Qu
E-mail(s) kqu@stanford.edu
Organization name Stanford University
Department Dermatology
Lab Howard Chang
Street address 269 Campus Dr. CCSR 2150
City Stanford
State/province CA
ZIP/Postal code 94305
Country USA
 
Platform ID GPL11154
Series (1)
GSE50676 Landscape and variation of RNA secondary structure across the human transcriptome
Relations
BioSample SAMN02350647
SRA SRX346863

Supplementary file Size Download File type/resource
GSM1226165_norm.rdGM12878_rep1_S1.tab.gz 1.4 Mb (ftp)(http) TAB
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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