|
Status |
Public on Sep 30, 2014 |
Title |
cultured cells sample 5 (T10-5) |
Sample type |
SRA |
|
|
Source name |
888mel melanoma cells
|
Organism |
Homo sapiens |
Characteristics |
biological sample: cells cultured in vitro for 10 days
|
Treatment protocol |
no treatment
|
Growth protocol |
subcutaneous tumors or cells grown in vitro with regular media
|
Extracted molecule |
genomic DNA |
Extraction protocol |
genomic DNA extracted using DNeasy Blood and Tissue kit (Quiagen). Samples were divided into half-samples and shRNAs were PCR amplified using a common reverse primer (5’-CAAGCAGAAGACGGCATACGAGATTTCTTTCCCCTGCACTGTACCC-3’) and unique forward primers, containing different 5 base-pairs index sequences, to distinguish between samples (5’-ACACTCTTTCCCTACACGACGCTCTTCCGATCTINDEXCTTGTGGAAAGGACGAAACACCGG-3’). After a second round of PCR, all PCR products were pooled and purified (QIAquick PCR Purification Kit - QIAGEN) and submitted to next generation sequencing (Illumina HiSeq2000). TRC-Hs1.0 kinome and related factors
|
|
|
Library strategy |
OTHER |
Library source |
other |
Library selection |
other |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
shRNA library
|
Data processing |
Count data was normalized with DESeq in R per pool. Pools (n=4) were merged after normalisation. Genome_build: hg19 Supplementary_files_format_and_content: Matrix with normalised count data
|
|
|
Submission date |
Sep 28, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Oscar Krijgsman |
E-mail(s) |
o.krijgsman@nki.nl, oscarkrijgsman@gmail.com
|
Phone |
31205122028
|
Organization name |
Netherlands Cancer Institute
|
Department |
Molecular Oncology and Immunology
|
Lab |
Peeper
|
Street address |
Plesmanlaan 121
|
City |
Amsterdam |
State/province |
Outside the US or Canada |
ZIP/Postal code |
1066CX |
Country |
Netherlands |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE61826 |
PARALLEL IN VIVO AND IN VITRO MELANOMA RNAi DROPOUT SCREENS |
|
Relations |
BioSample |
SAMN03083529 |
SRA |
SRX713876 |