基于DNA的疾病预测途径分析

Syeeda Farah, M. Sushma, T. Asha, B. Cauvery, K.S. Shivanand
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引用次数: 1

摘要

大多数疾病不是由单个基因组引起的,而是由多个基因组组合引起的。在患病样本中比在健康样本中更频繁出现的序列表明该疾病的一般因素。DNA已经成为预测疾病的非常有用的工具。通过允许医学专业人员识别DNA中作为疾病标记的基因,一个人可以做出适当的生活方式或类似的改变,以帮助降低患病风险。我们提出了一个系统,在该系统中,如果致病基因或相关基因发生突变,则通过确定疾病发生的概率水平来提供上述知识。
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DNA Based Disease Prediction Using Pathway Analysis
Most diseases are not triggered by a single genome but by a combination of genomes together. Sequences occurring more frequently in the diseased samples than in the healthy samples indicate the generic factors of the disease. DNA has become an extremely useful tool for predicting disease. By allowing medical professionals to identify genes in DNA that are markers for diseases, a person can make appropriate lifestyle or similar modifications to help lower the risk of disease. We propose a system in which the above knowledge is provided by determining the probabilistic levels of a disease occurring if the causal gene or the associated genes are mutated.
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