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首页> 外文期刊>Human Reproduction >Diagnostic accuracy: theoretical models for preimplantation genetic testing of a single nucleus using the fluorescence in situ hybridization technique.
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Diagnostic accuracy: theoretical models for preimplantation genetic testing of a single nucleus using the fluorescence in situ hybridization technique.

机译:诊断准确性:使用荧光原位杂交技术对单个核进行植入前遗传测试的理论模型。

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BACKGROUND: The aim of this study was to develop and use theoretical models to investigate the accuracy of the fluorescence in situ hybridization (FISH) technique in testing a single nucleus from a preimplantation embryo without the complicating effect of mosaicism. METHODS: Mathematical models were constructed for three different applications of FISH in preimplantation genetic testing (sex determination for sex-linked diseases, two-way reciprocal translocations and sporadic chromosome aneuploidy). The input values were the degree of aneuploidy (initially set at 3% per chromosome for sporadic aneuploidy) and the accuracy per probe (initially set at 95%), defined as the proportion of normal diploid nuclei with a normal signal pattern. The primary statistic was the predictive value of the test result. RESULTS: Testing two chromosome pairs to determine sex chromosome status or detect unbalanced translocation products had high predictive value: at least 99.5% for a normal test result (95% CI: 99-100%), and 90% for an abnormal test result (95% CI: 88-92%). However, the predictive value of an abnormal test result testing five chromosomes for sporadic chromosome aneuploidy was 41% (95% CI: 36-46%); 90% would be achieved with an aneuploidy rate per chromosome of 20.3% (equivalent to 99.5% prevalence for 23 chromosomes) rather than 3%, or with an accuracy per probe of 99.6% rather than 95%, or when testing 23 chromosome pairs, rather than 5 pairs, with either 8.3% aneuploidy (86.4% prevalence) or 99.5% accuracy. CONCLUSIONS: Testing a single cell using the FISH technique has the potential to achieve acceptable analytical performance for sex determination and two-way reciprocal translocations, but is unlikely to achieve adequate performance testing for sporadic chromosome aneuploidy. New techniques for detecting the copy number of every chromosome are emerging, but it remains to be seen if the high accuracy required will be achieved.
机译:背景:这项研究的目的是开发和使用理论模型来研究荧光原位杂交(FISH)技术在测试植入前胚胎中单个核而没有复杂镶嵌效果的准确性。方法:针对FISH在植入前基因测试中的三种不同应用(针对性相关疾病的性别确定,双向双向易位和零星染色体非整倍性)构建了数学模型。输入值是非整倍性的程度(对于散发性非整倍性,最初设置为每个染色体3%)和每个探针的准确性(初始设置为95%),定义为具有正常信号模式的正常二倍体核的比例。主要统计数据是测试结果的预测值。结果:测试两个染色体对以确定性染色体状态或检测不平衡的易位产物具有较高的预测价值:正常测试结果至少为99.5%(95%CI:99-100%),异常测试结果为90%( 95%CI:88-92%)。然而,测试五条染色体的零星非整倍性的异常测试结果的预测值为41%(95%CI:36-46%);每条染色体的非整倍体率为20.3%(相当于23条染色体的患病率是99.5%),而不是3%,或者每个探针的准确率为99.6%而不是95%,或者测试23条染色体对时,将达到90%。而不是5对,其非整倍性为8.3%(患病率为86.4%)或准确度为99.5%。结论:使用FISH技术测试单个细胞有可能实现可接受的性别确定和双向双向易位的分析性能,但不太可能实现散发染色体非整倍性的足够性能测试。检测每条染色体拷贝数的新技术正在兴起,但能否实现所需的高精度仍有待观察。

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