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Applications of Noninvasive Prenatal Testing for Subchromosomal Copy Number Variations Using Cell-Free DNA

Jiale Xiang1, Zhiyu Peng1

  • 1BGI Genomics, BGI-Shenzhen, Shenzhen 518083, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.

Clinics in Laboratory Medicine
|November 11, 2022
PubMed
Abstract

No abstract available in PubMed .

Keywords:
Copy number variationMicrodeletionMicroduplicationNoninvasive prenatal testingPrenatal screeningSubchromosomal abnormalities

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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