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Status |
Public on Feb 07, 2018 |
Title |
aCGH of chromosome X in a female patient with ALL and Leri-Weill syndrome |
Organism |
Homo sapiens |
Experiment type |
Genome variation profiling by SNP array Genome variation profiling by genome tiling array SNP genotyping by SNP array
|
Summary |
Array CGH of gDNA extracted from leukemic cells at diagnosis of ALL. Goal was to determine CNV polymorphisms linked with phenotype of ALL and Leri-Weill syndrome.
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Overall design |
ALL cells vs. reference genome control gDNA sample. Biological replicates: 1.
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Contributor(s) |
Urbankova H, Jarosova M |
Citation(s) |
29469136 |
|
Submission date |
Feb 06, 2018 |
Last update date |
May 09, 2018 |
Contact name |
Petr Vojta |
Organization name |
Palacky University
|
Department |
Laboratory of experimental medicine
|
Street address |
Hnevotinska 5
|
City |
Olomouc |
ZIP/Postal code |
77900 |
Country |
Czech Republic |
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Platforms (1) |
GPL24589 |
Agilent-029830 SurePrint G3 Human CGHplusSNP Microarray 4X180K G4890A |
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Samples (1) |
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Relations |
BioProject |
PRJNA433231 |