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Sample GSM1636061 Query DataSets for GSM1636061
Status Public on Feb 12, 2016
Title "default" NC, biological rep 2 of 3
Sample type SRA
 
Source name embryonic stem cells
Organism Homo sapiens
Characteristics differentiation day: day 12
Extracted molecule total RNA
Extraction protocol RNA was extracted with Trizol and cleaned up using a Qiagen RNEasy column
RNA libraries were prepared for sequencing using standard Illumina protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Data processing Illumina Casava1.7 software used for basecalling.
Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to hg19 whole genome using Tophat v1.3.3 with these parameters: -p8 -r 180 --library-type fr-unstranded --no-coverage-search --no-novel-juncs
Analysis with DESeq
Genome_build: hg19
Supplementary_files_format_and_content: Tab delimited file with DESeq output with fold change compared to CNS samples are provided.
 
Submission date Mar 18, 2015
Last update date May 15, 2019
Contact name Lorenz Studer
Organization name Memorial Sloan Kettering Cancer Center
Department Developmental Biology
Street address 430 E. 67th St. RRL 945
City New York
State/province NY
ZIP/Postal code 10021
Country USA
 
Platform ID GPL11154
Series (1)
GSE66148 RNA Sequencing of default, melanocyte biased and enteric human neural crest populations (NC) and neuroectoderm (CNS)
Relations
BioSample SAMN03430675
SRA SRX958156

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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