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UPDtool:一种利用 SNP 微阵列检测亲子三体型中同型和异型单体性的工具。

UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarrays.

机构信息

Department of Medical Genetics, University of Tübingen, Calwerstr. 7, 72076 Tübingen, Germany.

出版信息

Bioinformatics. 2013 Jun 15;29(12):1562-4. doi: 10.1093/bioinformatics/btt174. Epub 2013 Apr 14.

Abstract

UNLABELLED

UPDtool is a computational tool for detection and classification of uniparental disomy (UPD) in trio SNP-microarray experiments. UPDs are rare events of chromosomal malsegregation and describe the condition of two homologous chromosomes or homologous chromosomal segments that were inherited from one parent. The occurrence of UPD can be of major clinical relevance. Though high-throughput molecular screening techniques are widely used, detection of UPDs and especially the subclassification remains complex. We developed UPDtool to detect and classify UPDs from SNP microarray data of parent-child trios. The algorithm was tested using five positive controls including both iso- and heterodisomic segmental UPDs and 30 trios from the HapMap project as negative controls. With UPDtool, we were able to correctly identify all occurrences of non-mosaic UPD within our positive controls, whereas no occurrence of UPD was found within our negative controls. In addition, the chromosomal breakage points could be determined more precisely than by microsatellite analysis. Our results were compared with both the gold standard, microsatellite analysis and SNPtrio, another program available for UPD detection. UPDtool is platform independent, light weight and flexible. Because of its simple input format, UPDtool may also be used with other high-throughput technologies (e.g., next-generation sequencing).

AVAILABILITY AND IMPLEMENTATION

UPDtool executables, documentation and examples can be downloaded from http://www.uni-tuebingen.de/uni/thk/de/f-genomik-software.html.

摘要

未标记

UPDtool 是一种用于在 trio SNP 微阵列实验中检测和分类单亲二倍体(UPD)的计算工具。UPD 是染色体错误分离的罕见事件,描述了两条同源染色体或来自同一亲本的同源染色体片段的遗传情况。UPD 的发生可能具有重要的临床意义。尽管高通量分子筛选技术得到了广泛应用,但 UPD 的检测,特别是分类仍然很复杂。我们开发了 UPDtool 来从 SNP 微阵列数据的父母-子女三家中检测和分类 UPD。该算法使用包括同型和异型片段 UPD 在内的五个阳性对照进行了测试,并使用 HapMap 项目的 30 个三对作为阴性对照。使用 UPDtool,我们能够正确识别我们阳性对照中所有非嵌合 UPD 的发生情况,而在我们的阴性对照中未发现 UPD 的发生。此外,与微卫星分析相比,染色体断裂点的确定更加精确。我们的结果与金标准微卫星分析和 SNPtrio 进行了比较,后者是另一种可用于 UPD 检测的程序。UPDtool 是独立于平台的、轻量级的和灵活的。由于其简单的输入格式,UPDtool 也可以与其他高通量技术(例如下一代测序)一起使用。

可用性和实现

UPDtool 可执行文件、文档和示例可从 http://www.uni-tuebingen.de/uni/thk/de/f-genomik-software.html 下载。

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