系统评价DNA辅助技术在分子医学中的意义及其在全基因组研究中的应用

F. Khatoon, Reem A Alshammari, Aasma Batool, A. Elhaj, F. Alreshidi, G. Elhussein, R. A. Abdalla, A. B. M. Elhag, Z. Balouch
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引用次数: 0

摘要

目的:探讨分子DNA、DNA表型和聚合酶链反应在遗传调查相关样品中的作用。脱氧核糖核酸(DNA)是一种大分子,它推动了我们在细胞水平上理解生物体功能的能力,生物体如何繁殖和复制,以及将其主观遗传信息从一代传递到另一代。DNA也被称为生物体的遗传“蓝图”,并被发现拥有与特定存在有关的所有信息。核DNA存在于细胞核内,对细胞产生免疫具有重要意义,并取决于其框架内所包含的信息。线粒体DNA以2到10个拷贝的频率存在于线粒体内的不同位置。在分子医学实验室中最常见的体液是血液、精液和唾液,此外还有阴道分泌物、尿液和汗液。骨骼、牙齿、软组织等也是dna表型的重要生物标志物。研究方法:本研究的研究方法是对相关文献进行综述,以研究分子遗传学以及基因组和dna扩增在分子医学研究中的应用。要进行文献综述,质性研究设计是最合适的研究设计。它为评估人类行为提供了理论依据,并有助于使从二手来源有选择地收集的数据合法化和认证。结果:每个个体的DNA都由微小的改变组成,这些限制位点的变化会导致限制片段的不同剖面。基因组广泛的群体亚结构足够大,可以在大陆分辨率水平上确定具有大量常染色体snp的祖先。结论:人类基因组学和分子遗传学的发展为确定细胞起源和估计样本年龄和处置时间提供了成功和进步。在刑事案件中,像头发和眼睛颜色这样的表型特征已经产生了更好的推断,然而,DNA表型说明了一种有限的方法,其中纳入了生物材料分析。DNA技术的准确性对于分子医学领域的律师、人类学家、凶杀案侦探等专业人士来说非常有用,预计在未来几年还会有所提高。关键字;脱氧核糖核酸(DNA)、聚合酶链反应(PCR)、线粒体DNA (mtDNA)测序和短步重复序列(STR)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systematic Review on Implication for DNA Assisted Technology into Molecular Medicine and the useful is the application of Genome Wide Studies
Objective: The aim of this study is to explore the role of molecular DNA, DNA Phenotyping and Polymerase Chain Reaction in samples relevant to genetic investigation. The Deoxyribonucleic Acid (DNA) is a macromolecule which has propelled our capacity of understanding the function of an organism at the cellular level, how organism reproduce and replicate, and pass their subjective genetic information from one generation to the other. DNA is also referred to as the genetic “Blueprint” of an organism and found to possess all information pertaining to the specific being. Nuclear DNA is present within the nucleus and is significant in developing immunity for the cell and depends on the information incorporated within its framework. Mitochondrial DNA exists in varying locations in frequencies of two to ten copies within mitochondria. The most familiar body fluids come across in molecular medicine laboratories is blood, semen and saliva and further more are vaginal fluids, urine and sweat. Bones, teeth, soft tissues etc. are also essential biomarkers for DNA-phenotyping. Methodology: The methods for research for this particular study is to demonstrate a review of relevant literature to examine the molecular genetics and the application of genome and DNA-amplification into molecular medicine investigations. To conduct a literature review a qualitative research design is the most suitable research design. It provides the rationale for assessing the human behaviour and assists to legalize and authenticate the data which is selectively collected from the secondary sources. Results: Every individual’s DNA consists of minor alterations a change in these restriction places would result in different profile of restriction fragments. Genome wide population substructure is large enough to determine ancestry with large number of Autosomal SNPs at the level of continental resolutions. Conclusion: The advances in human genomics and molecular genetics have provided success and advances by determining the cellular origin and estimating the age of sample and disposition time. The Phenotypical characteristics like hair and eye color demonstration in criminal cases has yielded better inferences however, DNA phenotyping illustrates a limited approach wherein incorporated into biological material analysis. The accuracy of DNA technology is incredibly useful for professionals like lawyers, anthropologists, homicide detectives etc. in the field of molecular medicines and is expected to improve in years to come. Key Words; Deoxyribonucleic Acid (DNA) , Polymerase Chain Reaction (PCR), Mitochondrial DNA (mtDNA) sequencing and Short Tardem Repeat (STR)
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