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GenoWatch: a disease gene mining browser for association study.

机译:GenoWatch:用于关联研究的疾病基因挖掘浏览器。

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摘要

A human gene association study often involves several genomic markers such as single nucleotide polymorphisms (SNPs) or short tandem repeat polymorphisms, and many statistically significant markers may be identified during the study. GenoWatch can efficiently extract up-to-date information about multiple markers and their associated genes in batch mode from many relevant biological databases in real-time. The comprehensive gene information retrieved includes gene ontology, function, pathway, disease, related articles in PubMed and so on. Subsequent SNP functional impact analysis and primer design of a target gene for re-sequencing can also be done in a few clicks. The presentation of results has been carefully designed to be as intuitive as possible to all users. The GenoWatch is available at the website http://genepipe.ngc.sinica.edu.tw/genowatch
机译:人类基因关联研究通常涉及几种基因组标记,例如单核苷酸多态性(SNP)或短串联重复多态性,并且在研究过程中可能会鉴定出许多具有统计学意义的标记。 GenoWatch可以批量地从许多相关的生物学数据库中实时高效地提取有关多个标记及其相关基因的最新信息。检索到的全面基因信息包括基因本体,功能,途径,疾病,PubMed中的相关文章等。只需单击几下,即可进行后续SNP功能影响分析和目标基因的引物设计以进行重测序。结果的表示经过精心设计,对所有用户都尽可能直观。 GenoWatch可从以下网站获得:http://genepipe.ngc.sinica.edu.tw/genowatch

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