use of aCGH in a large series of prenatal samples
Source: NCBI BioProject (ID PRJNA136391)
Source: NCBI BioProject (ID PRJNA136391)
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Project name: Homo sapiens
Description: we have conducted a comparative study of the different technologies available for the detection of chromosomal abnormalities in prenatal samples. Here we include results of the aCGH experimentsOverall design: this series is composed of internal controls plus a year-long (2009-2010) consecutive series of pregnant women with indication for prenatal screening of chromosomal abnormalitiesa pdf and txt version of the table with 'sample name' plus relevant sample characteristics, including chromosomal abnormalities identified in our work is provided as a supplementary file on the Series record (below).
Data type: Variation
Sample scope: Multiisolate
Relevance: Medical
Organization: qGenomics
Literatures
- PMID: 21975797
Last updated: 2011-01-17