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Medline search engine for finding genetic markers with biological significance

机译:Medline搜索引擎,用于寻找具有生物学意义的遗传标记

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摘要

Motivation: Genome-wide high density SNP association studies are expected to identify various SNP alleles associated with different complex disorders. Understanding the biological significance of these SNP alleles in the context of existing literature is a major challenge since existing search engines are not designed to search literature for SNPs or other genetic markers. The literature mining of gene and protein functions has received significant attention and effort while similar work on genetic markers and their related diseases is still in its infancy. Our goal is to develop a web-based tool that facilitates the mining of Medline literature related to genetic studies and gene/protein function studies. Our solution consists of four main function modules for (1) identification of different types of genetic markers or genetic variations in Medline records (2) distinguishing positive versus negative linkage or association between genetic markers and diseases (3) integrating marker genomic location data from different databases to enable the retrieval of Medline records related to markers in the same linkage disequilibrium region (4) and a web interface called MarkerInfoFinder to search, display, sort and download Medline citation results. Tests using published data suggest MarkerInfoFinder can significantly increase the efficiency of finding genetic disorders and their underlying molecular mechanisms. The functions we developed will also be used to build a knowledge base for genetic markers and diseases.
机译:动机:全基因组高密度SNP关联研究有望确定与不同复杂疾病相关的各种SNP等位基因。在现有文献的背景下了解这些SNP等位基因的生物学意义是一项重大挑战,因为现有的搜索引擎并非旨在为SNP或其他遗传标记物搜索文献。有关基因和蛋白质功能的文献挖掘受到了极大的关注和努力,而有关遗传标记及其相关疾病的类似工作仍处于起步阶段。我们的目标是开发一个基于Web的工具,以促进与遗传研究和基因/蛋白质功能研究有关的Medline文献的挖掘。我们的解决方案包含四个主要功能模块,这些模块用于(1)识别Medline记录中不同类型的遗传标记或遗传变异(2)区分遗传标记与疾病之间的正向或负向联系或关联(3)整合来自不同标记的基因组位置数据数据库,以检索与同一连锁不平衡区域中的标记相关的Medline记录(4),以及一个称为MarkerInfoFinder的Web界面来搜索,显示,排序和下载Medline引用结果。使用公开数据进行的测试表明,MarkerInfoFinder可以显着提高发现遗传疾病及其潜在分子机制的效率。我们开发的功能还将用于建立遗传标记和疾病的知识库。

著录项

  • 来源
    《Bioinformatics》 |2007年第18期|2477-2484|共8页
  • 作者单位

    Molecular and Behavioral Neuroscience Institute and Department of Psychiatry University of Michigan Ann Arbor Michigan 48109 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 01:14:26

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