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Advantages of the single nucleotide polymorphism-based noninvasive prenatal test
Journal of Genetic Medicine ; : 66-71, 2015.
Artigo em Inglês | WPRIM | ID: wpr-195769
ABSTRACT
Down syndrome screening with cell-free DNA (cfDNA) in the maternal plasma has recently received much attention in the prenatal diagnostic field. Indeed, a large amount of evidence has already accumulated to show that screening tests with cfDNA are more sensitive and specific than conventional maternal serum and/or ultrasound screening. Globally, more than 1,000,000 of these noninvasive prenatal tests (NIPTs) have been performed to date. There are several different methods for NIPTs that are currently commercially available, including shotgun massively parallel sequencing, targeted massively parallel sequencing, and single nucleotide polymorphism (SNP)-based methods. All of these methods have their own advantages and disadvantages. In this review, I will focus specifically on the SNP-based NIPT.
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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Plasma / Diagnóstico Pré-Natal / DNA / Programas de Rastreamento / Ultrassonografia / Síndrome de Down / Polimorfismo de Nucleotídeo Único / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Estudo diagnóstico / Estudo de rastreamento Idioma: Inglês Revista: Journal of Genetic Medicine Ano de publicação: 2015 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Plasma / Diagnóstico Pré-Natal / DNA / Programas de Rastreamento / Ultrassonografia / Síndrome de Down / Polimorfismo de Nucleotídeo Único / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Estudo diagnóstico / Estudo de rastreamento Idioma: Inglês Revista: Journal of Genetic Medicine Ano de publicação: 2015 Tipo de documento: Artigo