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Status |
Public on Dec 24, 2020 |
Title |
amniotic fluid fetal cells 32 |
Sample type |
genomic |
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Source name |
amniotic fluid fetal cells
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Organism |
Homo sapiens |
Characteristics |
cell type: amniotic fluid fetal cells diagnosis: microdeletion of 16p12.2
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Treatment protocol |
N/A
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Growth protocol |
N/A
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Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA of fetal cells in amniotic fluid or cord blood sampling was extracted with using the QIAamp DNA extraction kit (Qiagen, Dusseldorf, Germany)
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Label |
Biotin
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Label protocol |
As per manufacturer (Affymetrix)
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|
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Hybridization protocol |
DNA was processed as follows. Restriction digested, PCR amplified, fragmented, labeled and hybridized to each array according to the manufacturer`s instructions.
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Scan protocol |
The arrays were then washed using Affymetrix Fluidics Stations, and scanned using the GeneChip Scanner 750K
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Description |
Hybridized to CytoScan 750K
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Data processing |
The array image was acquired using Affymetrix GeneChip® Command Console (AGCC version 4.0.0.1567). Data processing and analysis (CEL file generation, smoothing and segmentation) were used Chromosome Analysis Suite (version 3.3). Copy number variation status (CNV)
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Submission date |
Dec 23, 2020 |
Last update date |
Dec 24, 2020 |
Contact name |
Hailong Huang |
Organization name |
Fujian Maternity and Child Health Hospital
|
Street address |
No.18 Daoshan Road, Gulou District
|
City |
Fuzhou |
State/province |
Fujian |
ZIP/Postal code |
350001 |
Country |
China |
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|
Platform ID |
GPL18637 |
Series (1) |
GSE163799 |
Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers |
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