Targeted interrogation of copy number variation using SCIMMkit.

Targeted interrogation of copy number variation using SCIMMkit.
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使用SCIMMKIT对拷贝数变化的有针对性询问。

DOI:
10.1093/bioinformatics/btp606
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发表时间:
2010-01-01
期刊:
影响因子:
5.8
通讯作者:
Nickerson, Deborah A.
Nickerson, Deborah A.
中科院分区:
生物学3区
文献类型:
--
作者:
Zerr, Troy;Cooper, Gregory M.;Eichler, Evan E.;Nickerson, Deborah A.

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总结:拷贝数变异(Copy number variants,CNVs)对人类基因组多样性有重要贡献,开发准确有效的CNV基因分型方法是探索人类基因型-表型相关性的核心问题。SCIMMkit提供了三种先前验证的算法[SCIMM(SNP-条件混合建模),SCIMM-搜索和SCOUT(SNP-条件离群值检测)]的强大集成实现,用于使用Illumina Infinium II和GoldenGate SNP检测进行CNV的靶向询问。SCIMMkit适用于标准化的全基因组SNP阵列和定制化的多重SNP面板,为实验设计提供经济、高效和灵活性。可用性:源代码和文档可在http://droog.gs.washington.edu/scimmkit上用于非商业用途。联系方式:troyz@u.washington.edu补充信息:补充数据可从生物信息学在线网站获得。
Summary: Copy number variants (CNVs) contribute substantially to human genomic diversity, and development of accurate and efficient methods for CNV genotyping is a central problem in exploring human genotype–phenotype associations. SCIMMkit provides a robust, integrated implementation of three previously validated algorithms [SCIMM (SNP-Conditional Mixture Modeling), SCIMM-Search and SCOUT (SNP-Conditional OUTlier detection)] for targeted interrogation of CNVs using Illumina Infinium II and GoldenGate SNP assays. SCIMMkit is applicable to standardized genome-wide SNP arrays and customized multiplexed SNP panels, providing economy, efficiency and flexibility in experimental design. Availability: Source code and documentation are available for noncommercial use at http://droog.gs.washington.edu/scimmkit. Contact: troyz@u.washington.edu Supplementary information: Supplementary data are available at Bioinformatics online.
DOI: 10.1038/ng.236
发表时间: 2008-10
期刊: NATURE GENETICS
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