无创产前检测中胎儿微缺失和单基因变异的生物信息学方法比较

IF 1.2 Q4 GENETICS & HEREDITY
Lizzy Teleboshe Paul, M. C. Ergoren
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引用次数: 0

摘要

产前检查提供了关于胎儿健康状况的重要信息,并建议更好的治疗。在过去的几十年里,使用绒毛膜绒毛取样和羊膜穿刺术进行产前检查是侵入性产前诊断方法的两种主要形式。然而,为了方便产前检查而不对胎儿造成任何危险,利用循环无细胞脱氧核糖核酸(DNA)的无创产前诊断方法已成为一种合适的产前诊断方法。本文综述了近年来用于分析胎儿DNA浓度的生物信息学方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Bioinformatics Approaches for Fetal Microdeletions and Monogenic Variations Estimation in Non-invasive Prenatal Testing
Prenatal testing provides crucial information about the health status of fetuses as well as recommending better treatment. For the past decades, prenatal testing using chorionic villus sampling and amniocentesis were the two majorly used forms of invasive prenatal diagnostic approaches. However, to facilitate prenatal testing without causing any danger to the fetus, the noninvasive prenatal diagnostic method, which uses circulating cell-free deoxyribonucleic acid (DNA), has become a suitable method of prenatal diagnosis. This review discusses the recent bioinformatics approaches used for analyzing fetal DNA concentration.
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来源期刊
Global Medical Genetics
Global Medical Genetics GENETICS & HEREDITY-
自引率
11.80%
发文量
30
审稿时长
14 weeks
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