E-MTAB-1725 - Comparative genomic hybridization by array of chorionic villi from foetuses diagnosed as euploid or aneuploid by routine cytogenetic analysis to evaluate the usefulness of the CGH+SNP array in clinical diagnosis

Status
Released on 23 January 2014, last updated on 3 June 2014
Organism
Homo sapiens
Samples (70)
Array (1)
Protocols (6)
Description
Products of conception that were diagnosed either euploid or aneuploid during routine cytogenetic analysis were analysed by a novel CGH+SNP array for the evaluation of its usefulness in clinical diagnostics.
Experiment types
comparative genomic hybridization by array, array platform comparison, clinical history, comparative genome hybridization
Contact
Citation
Diagnostic utility of novel combined CGH+SNP-Arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in spontaneous abortions. Stefanie Bug, Beate Solfrank, Felizitas Schmitz, Jana Pricelius, Mona Stecher, Sonja Bingemann, Birgit Becker, Andrew Craig, Marc Botcherby, Claudia Nevinny-Stickel-Hinzpeter.
MIAME
PlatformsProtocolsFactorsProcessedRaw
Files
Investigation descriptionE-MTAB-1725.idf.txt
Sample and data relationshipE-MTAB-1725.sdrf.txt
Raw data (1)E-MTAB-1725.raw.1.zip
Array designA-MEXP-2321.adf.txt
Links