|
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 |