|
Status |
Public on Aug 29, 2017 |
Title |
ChR2 |
Sample type |
SRA |
|
|
Source name |
SU-pcGBM2 primary tumor cells
|
Organism |
Homo sapiens |
Characteristics |
tissue: primary cell mechanically dissociated from patient brain tumor cell type: SU-pcGBM2 primary tumor cells
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was isloated using Trizol reagent RNA libraries were prepared for sequencing using standard Illumina protocols
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
We generate 179.62M reads (clusters) (passing filter) with one lane of 50bp paired-end read libraries were then sequenced on Illumina HiSeq2500 Reads were mapped to whole genome HG19 (UCSC) using TopHat For data analysis, we use Cufflinks for differential expression analysis. Genome_build: hg19 Supplementary_files_format_and_content: cufflinks output
|
|
|
Submission date |
Oct 21, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Humsa Venkatesh |
E-mail(s) |
humsav@stanford.edu
|
Phone |
4084217437
|
Organization name |
Stanford University
|
Department |
Neurology
|
Lab |
Michelle Monje
|
Street address |
265 Campus Drive - Monje Lab
|
City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
|
|
Platform ID |
GPL16791 |
Series (1) |
GSE62563 |
Neuronal activity promotes glioma growth |
|
Relations |
BioSample |
SAMN03121932 |
SRA |
SRX737205 |