在《人类孟德尔遗传在线》（OMIM）中搜索与人类疾病相关的基因座信息。
Searching Online Mendelian Inheritance in Man (OMIM) for information for genetic loci involved in human disease.
作者信息
Baxevanis Andreas D
机构信息
National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
出版信息
Curr Protoc Hum Genet. 2003 Feb;Chapter 9:Unit9.13. doi: 10.1002/0471142905.hg0913s35.
Online Mendelian Inheritance in Man (OMIM) is a non-sequence-based information resource that can be of tremendous use to genomics researchers, physicians, and patients. There are two main ways in which a user can search the OMIM database. One may choose to search the OMIM database directly from the NCBI home page, as described in this unit. Alternatively, OMIM can be downloaded and run on any internal site where the user may want to keep from submitting data across the Web or where a local installation would be otherwise advantageous. Support Protocol describes how to navigate through an OMIM record. Online Mendelian Inheritance in Man (OMIM) is a non-sequence-based information resource that can be of tremendous use to genom Mendelian Inheritance in Man (OMIM) is a non-sequence-based information resource that can be of tremendous use to genomics researchers, physicians, and patients.
《人类孟德尔遗传在线》（OMIM）是一个基于非序列的信息资源，对基因组学研究人员、医生和患者有极大的用处。用户搜索OMIM数据库主要有两种方式。一种可以像本单元所述，直接从美国国立医学图书馆国家生物技术信息中心（NCBI）主页搜索OMIM数据库。或者，可以下载OMIM并在任何内部站点运行，这样用户可以避免通过网络提交数据，或者在其他情况下本地安装会更有利。支持协议描述了如何浏览OMIM记录。《人类孟德尔遗传在线》（OMIM）是一个基于非序列的信息资源，对基因组学研究人员、医生和患者有极大的用处。《人类孟德尔遗传在线》（OMIM）是一个基于非序列的信息资源，对基因组学研究人员、医生和患者有极大的用处。
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