首页> 美国卫生研究院文献>G3: GenesGenomesGenetics >Genetic Mapping in Autohexaploid Sweet Potato with Low-Coverage NGS-Based Genotyping Data
【2h】

Genetic Mapping in Autohexaploid Sweet Potato with Low-Coverage NGS-Based Genotyping Data

机译:具有低覆盖基于NGS的基因分型数据的自身红脂蛋白甘薯的遗传映射

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Next-generation sequencing (NGS)-based genotyping methods can generate numerous genetic markers in a single experiment and have contributed to plant genetic mapping. However, for high precision genetic analysis, the complicated genetic segregation mode in polyploid organisms requires high-coverage NGS data and elaborate analytical algorithms. In the present study, we propose a simple strategy for the genetic mapping of polyploids using low-coverage NGS data. The validity of the strategy was investigated using simulated data. Previous studies indicated that accurate allele dosage estimation from low-coverage NGS data (read depth < 40) is difficult. Therefore, we used allele dosage probabilities calculated from read counts in association analyses to detect loci associated with phenotypic variations. The allele dosage probabilities showed significant detection power, although higher allele dosage estimation accuracy resulted in higher detection power. On the contrary, differences in the segregation patterns between the marker and causal genes resulted in a drastic decrease in detection power even if the marker and casual genes were in complete linkage and the allele dosage estimation was accurate. These results indicated that the use of a larger number of markers is advantageous, even if the accuracy of allele dosage estimation is low. Finally, we applied the strategy for the genetic mapping of autohexaploid sweet potato ( ) populations to detect loci associated with agronomic traits. Our strategy could constitute a cost-effective approach for preliminary experiments done performed to large-scale studies.
机译:基于单一实验的基因分型方法的下一代测序(NGS)可以产生许多遗传标记,并有助于植物遗传映射。然而,对于高精度的遗传分析,多倍体生物中的复杂遗传分离模式需要高覆盖NGS数据和精细分析算法。在本研究中,我们提出了一种使用低覆盖NGS数据的多倍体遗传映射的简单策略。使用模拟数据调查了策略的有效性。以前的研究表明,从低覆盖NGS数据(读取深度<40)的准确等级剂量估计很难。因此,我们使用从关联分析中的读数计算的等位基因剂量概率来检测与表型变化相关的基因座。等位基因剂量概率显示出显着的检测力,但等等的等量剂量估计精度导致更高的检测力。相反,即使标记和休闲基因处于完全连杆状态,即使标记物和休闲基因完全链接,也导致检测功率之间的分离模式的差异导致检测功率的急剧下降,并且等位基因剂量估计准确。这些结果表明,即使等质量估计的准确性低,也可以使用较大数量的标记是有利的。最后,我们应用了自身红外甘薯()群的遗传映射策略,以检测与农艺性状相关的基因座。我们的战略可以构成对大规模研究进行的初步实验的经济有效方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号