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Status |
Public on Oct 17, 2014 |
Title |
Application of CGH-array and SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause |
Organism |
Homo sapiens |
Experiment type |
Genome variation profiling by SNP array Genome variation profiling by array
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Summary |
This SuperSeries is composed of the SubSeries listed below.
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Overall design |
Refer to individual Series
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Citation missing |
Has this study been published? Please login to update or notify GEO. |
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Submission date |
Oct 16, 2014 |
Last update date |
Nov 27, 2018 |
Contact name |
Francisco Martinez |
E-mail(s) |
martinez_fracas@gva.es
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Organization name |
Hospital Universitari i Politecnic La Fe
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Department |
Unidad de Genetica
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Street address |
Avenida Campanar 21
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City |
Valencia |
State/province |
Valencia |
ZIP/Postal code |
46009 |
Country |
Spain |
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Platforms (3) |
GPL6801 |
[GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array |
GPL8841 |
Agilent-014950 Human Genome CGH Microarray 4x44K (Probe Name version) |
GPL19303 |
Agilent-035925 microSOPHIA3.0 (4X44K) |
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Samples (5)
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GSM1527005 |
Human Male with Syndromic Intellectual disability_SNP-array |
GSM1527006 |
Human Male with Syndromic Intellectual disability_1_CGH-array |
GSM1527007 |
Human Female with Syndromic Intellectual disability_1_CGH-array |
GSM1527008 |
Human Male with Syndromic Intellectual disability_2_CGH-array |
GSM1527009 |
Human Female with Syndromic Intellectual disability_2_CGH-array |
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This SuperSeries is composed of the following SubSeries: |
GSE62438 |
Application of SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause |
GSE62439 |
Application of CGH-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause |
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Relations |
BioProject |
PRJNA264094 |