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Mapping genes for osteoporosis--old dogs and new tricks.

机译:定位骨质疏松症的基因-老狗和新技巧。

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In stark contrast to its horticultural origins, modern genetics is an extremely technology-driven field. Almost all the major advances in the field over the past 20 years have followed technological developments that have permitted change in study designs. The development of PCR in the 1980s led to RFLP mapping of monogenic diseases. The development of fluorescent-tagged genotyping methods led to linkage mapping approaches for common diseases that dominated the 1990s. The development of microarray SNP genotyping has led to the genome-wide association study era of the new millennium. And now the development of next-generation sequencing technologies is about to open up a new era of gene-mapping, enabling many potential new study designs. This review aims to present the strengths and weaknesses of the current approaches, and present some new ideas about gene-mapping approaches that are likely to advance our knowledge of the genes involved in heritable bone traits such as bone mineral density (BMD) and fracture.
机译:与园艺起源形成鲜明对比的是,现代遗传学是一个技术驱动的领域。在过去的20年中,该领域几乎所有的重大进步都伴随着技术发展,从而允许研究设计发生变化。 PCR在1980年代的发展导致对单基因疾病的RFLP定位。荧光标记基因分型方法的发展导致了1990年代主导的常见疾病的连锁作图方法。微阵列SNP基因分型的发展导致了新千年的全基因组关联研究时代。现在,下一代测序技术的发展即将开启基因映射的新纪元,使许多潜在的新研究设计成为可能。这篇综述旨在介绍当前方法的优点和缺点,并提出一些有关基因映射方法的新想法,这些想法可能会增进我们对涉及可遗传性骨特性(如骨矿物质密度(BMD)和骨折)的基因的了解。

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