利用新工具SUPER-CAP开发序列捕获数据的巨大潜力

V. Ruggieri, Irantzu Anzar, Andreu Paytuví, Roberta Calafiore, R. A. Cigliano, W. Sanseverino, A. Barone
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引用次数: 7

摘要

摘要序列捕获方法的最新发展为增强数据生成以评估目标基因组区域的遗传变异提供了一种强有力的策略。在这里,我们提出了SUPER-CAP,一个生物信息学网络工具,旨在处理序列捕获数据,精细计算变异的等位基因频率,并建立捕获基因的基因型特异性序列。用于开发这种计算机策略的数据集由44个番茄地方品种的378个位点和相关调控区域组成。大约有14000个高质量的变异被发现。高覆盖深度(>40倍)和采用正确的过滤标准,鉴定出约4000个罕见变异和10个拷贝数变异不同的基因。我们还表明,该工具能够通过使用检测到的变体来重建每种基因型的基因型特异性序列。这样就可以评估同一蛋白质中多种变体的综合效应。SUPER-CAP的架构和功能使该软件适用于广泛的分析,包括SNP发现和挖掘。它的功能,加上处理大型数据集和有效检测序列变异的能力,使SUPER-CAP成为基因组学和育种目的的宝贵生物信息学工具。
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Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP
Abstract The recent development of Sequence Capture methodology represents a powerful strategy for enhancing data generation to assess genetic variation of targeted genomic regions. Here, we present SUPER-CAP, a bioinformatics web tool aimed at handling Sequence Capture data, fine calculating the allele frequency of variations and building genotype-specific sequence of captured genes. The dataset used to develop this in silico strategy consists of 378 loci and related regulative regions in a collection of 44 tomato landraces. About 14,000 high-quality variants were identified. The high depth (>40×) of coverage and adopting the correct filtering criteria allowed identification of about 4,000 rare variants and 10 genes with a different copy number variation. We also show that the tool is capable to reconstruct genotype-specific sequences for each genotype by using the detected variants. This allows evaluating the combined effect of multiple variants in the same protein. The architecture and functionality of SUPER-CAP makes the software appropriate for a broad set of analyses including SNP discovery and mining. Its functionality, together with the capability to process large data sets and efficient detection of sequence variation, makes SUPER-CAP a valuable bioinformatics tool for genomics and breeding purposes.
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