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SYSTEM AND METHOD FOR CLEANING NOISY GENETIC DATA AND USING GENETIC, PHENTOYPIC AND CLINICAL DATA TO MAKE PREDICTIONS

机译:清洁嘈杂的遗传数据并利用遗传,表型和临床数据进行预测的系统和方法

摘要

A system and method for determining the genetic data for one or a small set ofcells, or from fragmentary DNA, where a limited quantity of genetic data isavailable, and also for predicting likely phenotypic outcomes usingmathematical models and given genetic, phenotypic and/or clinical data of anindividual, and also relevant aggregated medical data consisting of genotypic,phenotypic, and/or clinical data from germane patient subpopulations. Geneticdata for the target individual is acquired and amplified using known methods,and poorly measured base pairs, missing alleles and missing regions arereconstructed using expected similarities between the target genome and thegenome of genetically related subjects.
机译:一种用于确定一个或一小批人的遗传数据的系统和方法细胞或来自片段DNA的基因数据有限的情况可用,也可用于预测可能的表型结果数学模型和给定的遗传,表型和/或临床数据个体以及相关的汇总医学数据,包括基因型,来自德国患者亚群的表型和/或临床数据。遗传的使用已知方法获取并放大目标个体的数据,碱基对测量不佳,等位基因缺失和区域缺失使用目标基因组与基因相关主题的基因组。

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