GSM2222313[Accession] - GEO DataSets

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Items: 3

Select item 2000839411.

Chromosomal microarray analysis for validation of the WGS-based CNV detection results in recurrent miscarriage couples

(Submitter supplied) In order to validate of CNV detection from low-coverage whole-genome sequencing in the blood samples from recurrent miscarriage couples, we employed a customized array Comparative Genomics Hybridization (aCGH, Agilent) approach as chromosomal microarray analysis (CMA) in present study for a cohort of 78 DNA samples from blood. CMA results were compared with low-coverage whole-genome sequencing detection results. more...

Organism:: Homo sapiens

Type:: Genome variation profiling by array

Platform:: GPL20899
78 Samples

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Accession:: GSE83941

ID:: 200083941

Analyze with GEO2R

Select item 1000208992.

Agilent-068656 human array [hg19]

(Submitter supplied) For Richard 022023 140724 G4126A Arrays of this design have barcodes that begin with 16068656 or 2568656 Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. The ID column represents the Agilent probe name. more...