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Sample GSM1275988 Query DataSets for GSM1275988
Status Public on Nov 22, 2014
Title patient 34_peripheral blood_250Ksty
Sample type genomic
 
Source name patient 34_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_Sty
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 GPL3720
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
MM34-BL_Call
MM34-BL_LOH

Data table
ID_REF VALUE MM34-BL_Call MM34-BL_LOH
SNP_A-1924152 -0.064252 AA 1.208313
SNP_A-1926388 0.085866 BB 1.919085
SNP_A-2287278 -0.073814 AA 0.142154
SNP_A-1869654 0.062297 AB 0
SNP_A-1874310 -0.595533 AA 0.355386
SNP_A-1873090 0.024461 BB 0.071077
SNP_A-4283085 -0.234182 AA 5.261889
SNP_A-4289673 -0.337967 AA 619.722107
SNP_A-4302122 -0.122979 BB 0.426463
SNP_A-4301875 0.121035 AB 0
SNP_A-2314407 -0.215654 BB 3.83817
SNP_A-4248707 -0.057191 AA 0.710772
SNP_A-4249208 -0.037222 AA 14.23494
SNP_A-4258427 0.119031 AB 0
SNP_A-4258590 0.086409 AA 6.541282
SNP_A-4281462 0.079534 BB 11.587742
SNP_A-4281770 0.127489 BB 11.587742
SNP_A-2021661 -0.020531 AA 0.071077
SNP_A-2049537 0.075818 AB 0
SNP_A-2047945 0.139503 AB 6.541282

Total number of rows: 238304

Table truncated, full table size 7960 Kbytes.




Supplementary file Size Download File type/resource
GSM1275988_Sty_MM34-BL.CEL.gz 24.9 Mb (ftp)(http) CEL
GSM1275988_Sty_MM34-BL.CHP.gz 603.3 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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