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Sample GSM453714 Query DataSets for GSM453714
Status Public on Jun 01, 2010
Title Congenital Hypothyroidism (CH) Patient 4654
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 -0.033 3885 398 2895 122 0
1_1_2_Buffer_PCR null 987 390 554 120 0
1_1_3_397B22 -0.095 7182 384 5217 120 0
1_1_4_Buffer_PCR null 382 387 119 122 -50
1_1_5_Buffer_PCR null 6733 377 5069 115 0
1_1_6_F0488J12 -0.122 10392 366 7519 110 0
1_1_7_N0413M21 -0.022 5655 364 4268 111 0
1_1_8_D2542F24 -0.047 6281 370 4693 117 0
1_1_9_N0137H06 0.021 5710 376 4444 124 0
1_1_10_N0673B19 -0.231 467 374 161 124 0
1_1_11_N0090E12(del) -0.027 565 381 263 117 0
1_1_12_N0097G03 null 373 374 113 117 -50
1_1_13_N1030C19 -0.044 8290 390 6283 133 0
1_1_14_N0345M21 null 367 395 111 131 -50
1_1_15_N0281A03 null 551 377 253 120 -100
1_1_16_N0771D21 -0.154 392 385 130 124 0
1_1_17_N0504D21 null 787 460 463 194 -100
1_1_18_N0490A23 -0.189 20655 379 14060 115 0
1_1_19_M2112G04 0.002 3766 382 2870 119 0
1_1_20_N0282F14 -0.287 442 389 140 124 0

Total number of rows: 41760

Table truncated, full table size 1751 Kbytes.




Supplementary file Size Download File type/resource
GSM453714_MC_6641_6642_r_Cy3_CH4654_Cy5_fpool_S77_120207.gpr.gz 3.6 Mb (ftp)(http) GPR
Processed data included within Sample table

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