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Series GSE110235 Query DataSets for GSE110235
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.
 
Overall design ALL cells vs. reference genome control gDNA sample. Biological replicates: 1.
 
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
 
Platforms (1)
GPL24589 Agilent-029830 SurePrint G3 Human CGHplusSNP Microarray 4X180K G4890A
Samples (1)
GSM2983060 ALL cells from bone marrow
Relations
BioProject PRJNA433231

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE110235_RAW.tar 17.6 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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