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本文引用的文献

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Automated inference of molecular mechanisms of disease from amino acid substitutions.从氨基酸替换自动推断疾病的分子机制。
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Structural and functional restraints in the evolution of protein families and superfamilies.蛋白质家族和超家族进化中的结构与功能限制因素
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Unfoldomics of human diseases: linking protein intrinsic disorder with diseases.人类疾病的展开组学:将蛋白质内在无序与疾病联系起来。
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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.全基因组关联位点对人类疾病和性状的潜在病因学及功能影响。
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Inferring novel disease indications for known drugs by semantically linking drug action and disease mechanism relationships.通过语义关联药物作用与疾病机制关系来推断已知药物的新疾病适应症。
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转化生物信息学的进展:用于寻找疾病基因的计算方法。

Advances in translational bioinformatics: computational approaches for the hunting of disease genes.

机构信息

University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA.

出版信息

Brief Bioinform. 2010 Jan;11(1):96-110. doi: 10.1093/bib/bbp048. Epub 2009 Dec 10.

DOI:10.1093/bib/bbp048
PMID:20007728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2810112/
Abstract

Over a 100 years ago, William Bateson provided, through his observations of the transmission of alkaptonuria in first cousin offspring, evidence of the application of Mendelian genetics to certain human traits and diseases. His work was corroborated by Archibald Garrod (Archibald AE. The incidence of alkaptonuria: a study in chemical individuality. Lancert 1902;ii:1616-20) and William Farabee (Farabee WC. Inheritance of digital malformations in man. In: Papers of the Peabody Museum of American Archaeology and Ethnology. Cambridge, Mass: Harvard University, 1905; 65-78), who recorded the familial tendencies of inheritance of malformations of human hands and feet. These were the pioneers of the hunt for disease genes that would continue through the century and result in the discovery of hundreds of genes that can be associated with different diseases. Despite many ground-breaking discoveries during the last century, we are far from having a complete understanding of the intricate network of molecular processes involved in diseases, and we are still searching for the cures for most complex diseases. In the last few years, new genome sequencing and other high-throughput experimental techniques have generated vast amounts of molecular and clinical data that contain crucial information with the potential of leading to the next major biomedical discoveries. The need to mine, visualize and integrate these data has motivated the development of several informatics approaches that can broadly be grouped in the research area of 'translational bioinformatics'. This review highlights the latest advances in the field of translational bioinformatics, focusing on the advances of computational techniques to search for and classify disease genes.

摘要

一个多世纪以前,William Bateson 通过对一级表亲后代中尿黑酸尿症遗传的观察,为孟德尔遗传学在某些人类特征和疾病中的应用提供了证据。他的工作得到了 Archibald Garrod(Archibald AE. The incidence of alkaptonuria: a study in chemical individuality. Lancert 1902;ii:1616-20)和 William Farabee(Farabee WC. Inheritance of digital malformations in man. In: Papers of the Peabody Museum of American Archaeology and Ethnology. Cambridge, Mass: Harvard University, 1905; 65-78)的证实,他们记录了人类手足畸形的家族遗传倾向。这些人是寻找疾病基因的先驱,这一探索将持续一个世纪,并发现数百个与不同疾病相关的基因。尽管上个世纪有许多开创性的发现,但我们远未完全理解疾病涉及的复杂分子过程网络,我们仍在寻找大多数复杂疾病的治疗方法。在过去的几年中,新的基因组测序和其他高通量实验技术产生了大量的分子和临床数据,其中包含有潜在潜力的关键信息,可以促成下一个重大的生物医学发现。挖掘、可视化和整合这些数据的需求推动了几种信息学方法的发展,这些方法可以广泛地归类于“转化生物信息学”研究领域。这篇综述强调了转化生物信息学领域的最新进展,重点介绍了计算技术在搜索和分类疾病基因方面的最新进展。