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Sample GSM453748 Query DataSets for GSM453748
Status Public on Jun 01, 2010
Title Congenital Hypothyroidism (CH) Patient 3698
Sample type genomic
 
Channel 1
Source name dna isolated from blood of a patient with ch. gender: female
Organism Homo sapiens
Characteristics tissue: blood of a patient with ch.
gender: female
Treatment protocol sonicated
Extracted molecule genomic DNA
Extraction protocol DNA was extracted from peripheral blood by QiaAmp DNA Blood Mini Kit Protocol.
Label Cy3
Label protocol Probes were labelled by random priming. Detailed protocols are available at our website (Molecular Cytogenetics at the Max Planck Institute for Molecular Genetics)
 
Channel 2
Source name DNA isolated from the blood of a donorpool of 5 healthy females.
Organism Homo sapiens
Characteristics tissue: blood of a donor pool of 5 healthy females.
gender: female
Treatment protocol sonicated
Extracted molecule genomic DNA
Extraction protocol DNA was extracted from peripheral blood by QiaAmp DNA Blood Mini Kit Protocol.
Label Cy5
Label protocol Probes were labelled by random priming. Detailed protocols are available at our website (Molecular Cytogenetics at the Max Planck Institute for Molecular Genetics)
 
 
Hybridization protocol Hybridization was done overnight at 42?C in a slide booster (Advalytix, Brunnthal, Germany). Detailed protocols are available at our website (Molecular Cytogenetics at the Max Planck Institute for Molecular Genetics)
Scan protocol Slides were scanned using an Agilent scanner . PMT settings: 100/100
Description Array CGH analysis of a patient with Congenital Hypothyroidism.
Data processing TIFF images were analysed by Genepix 5.0 (Axon Instruments, Union City, CA) and raw intensities (gpr files) were imported into CGHPRO (Chen at al.,2005). Background intensities were not substracted. Signal intensities were normalized by subgridd LOWESS. Aberrant ratios involving three or more neighbouring clones wereconsidered as genomic aberrations, unless they coincided with a known polymorphism as listed in the Database of Genomic Variants (version Dec 2005)
 
Submission date Sep 17, 2009
Last update date Mar 22, 2010
Contact name Reinhard Ullmann
E-mail(s) [email protected]
Phone 00493084131251
Organization name MPIMG
Department Human Molecular Genetics
Lab Molecular Cytogenetics
Street address Ihnestr.73
City Berlin
ZIP/Postal code 14195
Country Germany
 
Platform ID GPL5114
Series (1)
GSE18152 Screening for chromosomal aberrations by array CGH in 74 patients with congenital hypothyroidism

Data table header descriptions
ID_REF
VALUE normalized log ratio (subgrid lowess)
f635Mean foreground signal intensity Cy5
b635Mean background signal intensity Cy5
f532Mean foreground signal intensity Cy3
b532Mean background signal intensity Cy3
Flags 0: valid spots -50: clones with unverified chromosomal positions -100: excluded

Data table
ID_REF VALUE f635Mean b635Mean f532Mean b532Mean Flags
1_1_1_bK1444N24 0.053 1479 153 2955 72 0
1_1_2_Buffer_PCR null 774 156 1400 74 0
1_1_3_397B22 0.006 3090 158 6167 73 0
1_1_4_Buffer_PCR null 750 155 1402 69 0
1_1_5_Buffer_PCR null 2182 154 4264 70 0
1_1_6_F0488J12 0.029 3387 156 6877 70 0
1_1_7_N0413M21 0.062 1772 157 3588 71 0
1_1_8_D2542F24 -0.022 1573 160 2985 74 0
1_1_9_N0137H06 0.032 1476 157 2904 74 0
1_1_10_N0673B19 null 153 155 65 73 -50
1_1_11_N0090E12(del) -0.045 1567 157 2929 74 0
1_1_12_N0097G03 null 152 153 71 72 -50
1_1_13_N1030C19 -0.005 2386 156 4707 74 0
1_1_14_N0345M21 null 163 157 90 73 -50
1_1_15_N0281A03 0.046 2567 156 5260 83 0
1_1_16_N0771D21 -0.066 4643 159 8813 89 0
1_1_17_N0504D21 -0.018 2520 186 4931 135 0
1_1_18_N0490A23 -0.116 1485 300 2632 374 0
1_1_19_M2112G04 -0.017 1693 212 3232 194 0
1_1_20_N0282F14 null 185 178 144 116 -50

Total number of rows: 41760

Table truncated, full table size 1739 Kbytes.




Supplementary file Size Download File type/resource
GSM453748_MC_6803_6804_r_Cy3_CH3698_Cy5_fpool_S69_190906.gpr.gz 3.6 Mb (ftp)(http) GPR
Processed data included within Sample table

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