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Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing

机译:使用高通量微流控技术和下一代测序技术扩大针对犹太人群的孕前载体筛选

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摘要

BackgroundGenetic screening to identify carriers of autosomal recessive diseases has become an integral part of routine prenatal care. In spite of the rapid growth of known mutations, most current screening programs include only a small subset of these mutations, and are performed using diverse molecular techniques, which are generally labor-intensive and time consuming. We examine the implementation of the combined high-throughput technologies of specific target amplification and next generation sequencing (NGS), for expanding the carrier screening program in the Israeli Jewish population as a test case.
机译:背景技术进行基因筛查以鉴定常染色体隐性遗传疾病的携带者已成为常规产前保健的组成部分。尽管已知突变迅速增长,但大多数当前的筛选程序仅包括这些突变的一小部分,并且使用多种分子技术进行,这些技术通常是劳动密集型且耗时的。我们测试了特定靶标扩增和下一代测序(NGS)结合的高通量技术的实施情况,以作为测试用例在以色列犹太人口中扩展携带者筛查计划。

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