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Sample GSM566265 Query DataSets for GSM566265
Status Public on Apr 07, 2011
Title LAU-Me275 melanoma cells patient LAU50 (454)
Sample type SRA
 
Source name Low-passage culture of lymph node metastasis from cutaneous melanoma
Organism Homo sapiens
Characteristics gender: male
cell line: cell derived from metastatic melanoma
source tissue: lymph node
Treatment protocol none
Growth protocol Melanoma cell lines were cultured in RPMI-1640 medium supplemented with 10% FCS. Normal human melanocytes were grown in HAM-F10 medium supplemented with 2% FCS, 5% MelanoMax supplement (Gentaur, Belgium) and 6 mM HEPES.
Extracted molecule total RNA
Extraction protocol mRNA isolation and cDNA preparation were performed following the protocol used by Bainbridge et al (BMC Genomics. 2006 ). Then 3-5 µg of cDNA were used for 454 libraries preparation, according to manufactures’ procedures.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model 454 GS FLX
 
Description cDNA was sequenced using single end read with the Roche 454 technology
hg18 used for NHM_7Mel_mRNA_cnt.txt
Data processing All experiments produced about 1M single end reads, with a median length of 367 nucleotides (interquartile range 265-436). We derived transcript tag count using the Tromer pipeline described in Jongeneel et al. (PNAS 2003)
 
Submission date Jul 14, 2010
Last update date May 15, 2019
Contact name Armand Valsesia
Organization name Ludwig Institute for Cancer Research
Street address Bâtiment Génopode
City Lausanne
ZIP/Postal code 1015
Country Switzerland
 
Platform ID GPL9186
Series (2)
GSE22932 Genome-Wide Analysis of Somatic Copy Number Alterations and Gene Expression in Metastatic Melanoma: RNA-Seq
GSE23056 Genome-Wide Analysis of Somatic Copy Number Alterations and Gene Expression in Metastatic Melanoma
Relations
SRA SRX025092
BioSample SAMN00025389

Supplementary data files not provided
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA

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