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Sample GSM919924 Query DataSets for GSM919924
Status Public on May 04, 2012
Title Clutch1_Stage11-12_Set1
Sample type SRA
 
Source name embryo_stage 11-12
Organism Xenopus tropicalis
Characteristics strain: Outbred
clutch: 1
developmental stage: stage 11-12
tissue: embryo
Extracted molecule total RNA
Extraction protocol The general Illumina mRNA-Seq library preparation workflow was followed with some modifications. First, polyA-containing RNAs were selected. The RNAs were then fragmented in 5X First-Strand Buffer (Invitrogen) at 85oC for 7-8 minutes. Random hexamers and SuperScript III (Invitrogen) were used to synthesize the first strand cDNA. Second strand cDNA synthesis was performed with dUTP in place of dTTP to mark the second strand. After end repair and addition of adenosine to the 3'ends, standard Illumina adapters were ligated. DNA fragments in the size range of 300 to 600bp were gel extracted and treated with UDG before each library was amplified using Phusion (Finnzymes).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description polyA-selected RNA
Data processing Bowtie was used for alignment.
TopHat and SpliceMap were used for splice junction detection.
Cufflinks and Rseq were used to generate abundance measurements.
Genome_build: XenTro3
 
Submission date Apr 20, 2012
Last update date May 15, 2019
Contact name Kin Fai Au
E-mail(s) kinfai@stanford.edu
Organization name Stanford
Department Statistics
Street address James H. Clark Center, 1st Floor East, 318 Campus Drive,
City Stanford
ZIP/Postal code CA 94305
Country USA
 
Platform ID GPL15472
Series (1)
GSE37452 RNA sequencing reveals diverse and dynamic repertoire of the Xenopus tropicalis transcriptome over development.
Relations
SRA SRX143518
BioSample SAMN00861985

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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