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GENETICS AND GENOMICS OF CANCER

机译:癌症的遗传和基因组学

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There have been dramatic advances in our understanding of the genetic and basis of many cancers. This information is helping to develop new drugs and therapies in appropriate patients and the use of this knowledge is improving the outcome of patients with cancer. At the beginning of this century, international public and private efforts provided the sequence of the entire human genome. Examination of the data revealed that the genome consists of less than 25,000 genes. The completion of the sequence of the first canonical human genome was estimated to have cost $2.5 billion. During the last 15 years, the cost of sequencing the human genome has decreased dramatically. Many other technologies for assessing gene expression, epigenetic modification of DNA, assessment of the levels of micro RNA, levels of long non-coding RNA and accurate determination of the levels of individual proteins have evolved and improved. The availability of these diverse technologies enabled the launch of several new programs to decipher the genetic and genomic makeup of all the common tumor types around the world.
机译:我们对许多癌症的遗传和基础的理解有戏剧性的进步。这些信息有助于在适当的患者中开发新的药物和治疗,并且利用这种知识正在改善癌症患者的结果。在本世纪初,国际公共和私人努力提供了整个人类基因组的序列。检查数据显示,基因组由少于25,000个基因组成。估计第一个规范人类基因组的序列的完成成本为25亿美元。在过去的15年中,测序人类基因组的成本急剧下降。许多其他用于评估基因表达的技术,DNA的表观遗传修饰,微RNA水平评估,长的非编码RNA水平以及精确测定单个蛋白质的水平已经进化和改进。这些不同技术的可用性使得推出了几个新程序来破译世界各地所有常见肿瘤类型的遗传和基因组化妆。

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