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SNP2CAPS: a SNP and INDEL analysis tool for CAPS marker development

机译:SNP2CAPS:用于CAPS标记开发的SNP和INDEL分析工具

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With the influx of various SNP genotyping assays in recent years, there has been a need for an assay that is robust, yet cost effective, and could be performed using standard gel‐based procedures. In this context, CAPS markers have been shown to meet these criteria. However, converting SNPs to CAPS markers can be a difficult process if done manually. In order to address this problem, we describe a computer program, SNP2CAPS, that facilitates the computational conversion of SNP markers into CAPS markers. 413 multiple aligned sequences derived from barley ESTs were analysed for the presence of polymorphisms in 235 distinct restriction sites. 282 (90%) of 314 alignments that contain sequence variation due to SNPs and InDels revealed at least one polymorphic restriction site. After reducing the number of restriction enzymes from 235 to 10, 31% of the polymorphic sites could still be detected. In order to demonstrate the usefulness of this tool for marker development, we experimentally validated some of the results predicted by SNP2CAPS.
机译:近年来,随着各种SNP基因型分析方法的涌入,需要一种功能强大但又具有成本效益并且可以使用基于凝胶的标准程序进行分析的方法。在这种情况下,CAPS标记已显示满足这些标准。但是,如果手动完成,将SNP转换为CAPS标记可能是一个困难的过程。为了解决此问题,我们描述了一个计算机程序SNP2CAPS,该程序可促进SNP标记到CAPS标记的计算转换。分析了来自大麦ESTs的413个多个比对序列在235个不同的限制性酶切位点中多态性的存在。 314个比对中的282个(占90%)包含因SNP和InDel引起的序列变异,显示出至少一个多态性限制性位点。将限制酶的数量从235种减少到10种后,仍可检测到31%的多态性位点。为了证明该工具对标记物开发的有用性,我们通过实验验证了SNP2CAPS预测的一些结果。

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