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In silico whole-genome screening for cancer-related single-nucleotide polymorphisms located in human mRNA untranslated regions

机译:在计算机全基因组中筛选位于人类mRNA非翻译区的癌症相关单核苷酸多态性

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摘要

BackgroundA promising application of the huge amounts of genetic data currently available lies in developing a better understanding of complex diseases, such as cancer. Analysis of publicly available databases can help identify potential candidates for genes or mutations specifically related to the cancer phenotype. In spite of their huge potential to affect gene function, no systematic attention has been paid so far to the changes that occur in untranslated regions of mRNA.
机译:背景技术当前可获得的大量遗传数据的有希望的应用在于对复杂疾病(例如癌症)的更好理解。对公共数据库的分析可以帮助确定与癌症表型特别相关的基因或突变的潜在候选者。尽管它们具有潜在的影响基因功能的巨大潜力,但迄今为止,尚未对mRNA非翻译区中发生的变化进行系统的关注。

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