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Sample GSM453723 Query DataSets for GSM453723
Status Public on Jun 01, 2010
Title Healthy Patient 4796, mother of CH Patient 4619
Sample type genomic
 
Channel 1
Source name dna isolated from blood of a healthy patient. gender: female
Organism Homo sapiens
Characteristics tissue: blood of a healthy patient.
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 the healthy father of CH patient 4619
Organism Homo sapiens
Characteristics tissue: blood of the healthy father of CH patient 4619
gender: male
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 0.117 3101 279 5064 142 0
1_1_2_Buffer_PCR null 1671 281 2469 140 0
1_1_3_397B22 0.133 5864 282 10165 148 0
1_1_4_Buffer_PCR null 2039 282 3342 148 0
1_1_5_Buffer_PCR null 4195 271 6912 136 0
1_1_6_F0488J12 0.16 6145 268 10880 137 0
1_1_7_N0413M21 0.14 4144 267 7070 139 0
1_1_8_D2542F24 0.631 2204 263 5045 134 0
1_1_9_N0137H06 0.078 3091 264 4900 134 0
1_1_10_N0673B19 null 249 260 121 130 -50
1_1_11_N0090E12(del) 0.042 2738 254 4174 122 0
1_1_12_N0097G03 null 240 253 115 123 -50
1_1_13_N1030C19 -0.015 4623 246 7104 118 0
1_1_14_N0345M21 null 281 247 169 122 -100
1_1_15_N0281A03 -0.044 4908 248 7403 119 0
1_1_16_N0771D21 -0.047 7187 246 11003 115 0
1_1_17_N0504D21 -0.081 4629 257 6783 139 0
1_1_18_N0490A23 null 975 282 1241 188 -100
1_1_19_M2112G04 -0.081 3118 256 4405 129 0
1_1_20_N0282F14 null 237 248 113 115 -50

Total number of rows: 41760

Table truncated, full table size 1743 Kbytes.




Supplementary file Size Download File type/resource
GSM453723_MC_6939_6940_r_Cy3_CH4796_Cy5_CH4795_S78_190906.gpr.gz 3.7 Mb (ftp)(http) GPR
Processed data included within Sample table

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