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第14届国际人类白细胞抗原与免疫遗传学研讨会:方法学、数据收集及分析进展报告

14th International HLA and Immunogenetics Workshop: report of progress in methodology, data collection, and analyses.

作者信息

Single R M, Meyer D, Mack S J, Lancaster A, Erlich H A, Thomson G

机构信息

Department of Mathematics and Statistics, University of Vermont, Burlington, VT, USA.

出版信息

Tissue Antigens. 2007 Apr;69 Suppl 1:185-7. doi: 10.1111/j.1399-0039.2006.00767.x.

DOI:10.1111/j.1399-0039.2006.00767.x
PMID:17445197
Abstract

The Biostatistics Component of the 13th International Histocompatibility Workshop (IHWS) developed the PyPop (Python for Population Genomics) software framework for high-throughput analysis and quality control (QC) assessments of highly polymorphic genotype data. Since its initial release, the software has had several new analysis modules added to it. These additions, combined with improved data filtering and QC modules, facilitate analyses of data at different levels (allele, haplotype, amino acid sequence, and nucleotide sequence). Since the 13th IHWS, much of the human leukocyte antigen (HLA) data from the workshop, QCed via PyPop and other methods, have been made publicly available through the Major Histocompatibility Complex database web site at the National Center for Biotechnology Information (http://ncbi.nih.gov/mhc/). The Anthropology/Human Genetic Diversity component (AHGDC) data have been used in a variety of studies. Prugnolle et al. used this data to corroborate a model of pathogen-driven selection as a factor related to high levels of diversity at HLA loci. Using a comparative genomics approach contrasting results for HLA and non-HLA markers, Meyer et al. analyzed a subset of the 13th IHWS AHGDC data and showed that HLA loci show detectable signs of both natural selection and the demographic history of populations.

摘要

第13届国际组织相容性研讨会(IHWS)的生物统计学组成部分开发了PyPop(用于群体基因组学的Python)软件框架,用于对高度多态的基因型数据进行高通量分析和质量控制(QC)评估。自首次发布以来,该软件已添加了几个新的分析模块。这些新增模块与改进的数据过滤和QC模块相结合,便于对不同层面的数据(等位基因、单倍型、氨基酸序列和核苷酸序列)进行分析。自第13届IHWS以来,通过PyPop和其他方法进行质量控制的研讨会上的许多人类白细胞抗原(HLA)数据已通过美国国立生物技术信息中心的主要组织相容性复合体数据库网站(http://ncbi.nih.gov/mhc/)公开提供。人类学/人类遗传多样性组成部分(AHGDC)的数据已用于各种研究。普鲁尼奥勒等人利用这些数据证实了病原体驱动选择模型,该模型是与HLA基因座高水平多样性相关的一个因素。迈耶等人采用比较基因组学方法对比了HLA和非HLA标记的结果,分析了第13届IHWS AHGDC数据的一个子集,结果表明HLA基因座显示出自然选择和群体人口统计学历史的可检测迹象。

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