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Sample GSM1275967 Query DataSets for GSM1275967
Status Public on Nov 22, 2014
Title patient 21_peripheral blood_250Knsp
Sample type genomic
 
Source name patient 21_peripheral blood
Organism Homo sapiens
Characteristics cell: peripheral blood
Treatment protocol None
Growth protocol After centrifugation, primary cells in pleural effusions or ascites were cultured in -MEM (Invitrogen, Carlsbad, CA, USA) supplemented with 10% FBS (Equitech-Bio, Ingram, TX, USA). Surgically resected tumors were cut into small pieces. These pieces were plated on culture dishes and gently overlaid with culture medium. Primary outgrowth cells were cultured in -MEM–10% FBS. Adherent cells were expanded by several passages for several weeks or months.
Extracted molecule genomic DNA
Extraction protocol Genomic DNA from cultured cells were isolated with an AllPrep DNA/RNA mini kit (Qiagen, Hilden, Germany) following the manufacturer's protocol. Genomic DNA from peripheral blood was isolated with a QIAamp DNA Blood Mini Kit (Qiagen).
Label Biotin
Label protocol As per manufacturer (Affymetrix)
 
Hybridization protocol DNA was restriction digested, PCR amplified, fragmented, labeled and hybridized to each array according to the manufacturer's instructions.
Scan protocol The Arrays were then washed using Affymetrix fluidics stations, and scanned using the Gene Chip Scanner 3000.
Description Hybridized to 250K_Nsp
Data processing The probe intensities at each locus were determined in the Affymetrix GeneChip Operating System GCOS software, and genotype calls were generated using the Affymetrix Genotyping Console GTC Software (Version 3.0.2). Primary data analysis was performed using GTC software, and further statistical studies were analyzed using the CNAG (Copy Number Analyzer for Affymetrix GeneChip Mapping arrays) software, version 2.0 (Genome Laboratory, The University of Tokyo, http://www.genome.umin.jp) for Mapping 500K set. For SNP6.0 array, genotype calls were generated using the Affymetrix Genotyping Console GTC Software (Version 3.0.2) using birdseed version 2 algorithm with other 100 files.
Call (SNP call): AA, AB, BB, and NoCall; Log2Ratio: copy number log2 ratio between the test and reference samples of zero; LOH: posibility of loss of heterozygosity (bigger number means higher posibility of LOH for CNAG, but Genotyping Console gave 1 with posibility of LOH)
 
Submission date Nov 27, 2013
Last update date Nov 22, 2014
Contact name Yoshie Yoshikawa
E-mail(s) yoshiey@hyo-med.ac.jp
Phone +81-798-45-6587
Organization name Hyogo College of Medicine
Department Genetics
Street address 1-1 Mukogawa-cho
City Nishinomiya
State/province Hyogo
ZIP/Postal code 663-8501
Country Japan
 
Platform ID GPL3718
Series (1)
GSE52788 DNA copy number changes in malignant mesothelioma

Data table header descriptions
ID_REF
VALUE Log2Ratio: copy number log2 ratio between the test and reference samples of zero
MM21-BL_Call
MM21-BL_LOH

Data table
ID_REF VALUE MM21-BL_Call MM21-BL_LOH
SNP_A-1949834 -0.193305 AA 0.071077
SNP_A-1985629 -0.584068 AA 0.497541
SNP_A-1915140 -0.206512 AB 0
SNP_A-1915915 -0.102837 BB 0.355386
SNP_A-1914262 0.069701 AA 0.995081
SNP_A-4218271 -0.092058 AA 3.129568
SNP_A-4218854 0.115154 BB 0.142154
SNP_A-4218005 0.172551 AA 1.634777
SNP_A-4226293 -0.358988 BB 1.137236
SNP_A-4239338 0.042282 AA 2.345548
SNP_A-4238952 -0.122767 AB 0
SNP_A-2290352 0.403782 AA 0.355386
SNP_A-2290132 -0.180893 BB 3.83817
SNP_A-2292676 -0.25473 AA 11.727728
SNP_A-4193466 -0.019516 NoCall 0.142154
SNP_A-4193165 -0.512523 AB 0
SNP_A-4192925 -0.087827 BB 0.426463
SNP_A-4193647 -0.78245 AB 0
SNP_A-4193492 -0.085517 AB 0
SNP_A-4215529 -0.261625 AB 0

Total number of rows: 262264

Table truncated, full table size 8806 Kbytes.




Supplementary file Size Download File type/resource
GSM1275967_Nsp_MM21-BL.CEL.gz 25.2 Mb (ftp)(http) CEL
GSM1275967_Nsp_MM21-BL.CHP.gz 616.1 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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