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Detection of cytogenomic abnormalities by OncoScan microarray assay for products of conception from formalin-fixed paraffin-embedded and fresh fetal tissues
BACKGROUND: The OncoScan microarray assay (OMA) using highly multiplexed molecular inversion probes for single nucleotide polymorphism (SNP) loci enabled the detection of cytogenomic abnormalities of chromosomal imbalances and pathogenic copy number variants (pCNV). The small size of molecular inver...
Autores principales: | Wen, Jiadi, Grommisch, Brittany, DiAdamo, Autumn, Chai, Hongyan, Ng, Sok Meng Evelyn, Hui, Pei, Bale, Allen, Mak, Winifred, Wang, Guilin, Li, Peining |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019165/ https://www.ncbi.nlm.nih.gov/pubmed/33810806 http://dx.doi.org/10.1186/s13039-021-00542-5 |
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