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Two-Phase Analysis in Consensus Genetic Mapping

机译:共识遗传图谱的两阶段分析

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摘要

Numerous mapping projects conducted on different species have generated an abundance of mapping data. Consequently, many multilocus maps have been constructed using diverse mapping populations and marker sets for the same organism. The quality of maps varies broadly among populations, marker sets, and software used, necessitating efforts to integrate the mapping information and generate consensus maps. The problem of consensus genetic mapping (MCGM) is by far more challenging compared with genetic mapping based on a single dataset, which by itself is also cumbersome. The additional complications introduced by consensus analysis include inter-population differences in recombination rate and exchange distribution along chromosomes; variations in dominance of the employed markers; and use of different subsets of markers in different labs. Hence, it is necessary to handle arbitrary patterns of shared sets of markers and different level of mapping data quality. In this article, we introduce a two-phase approach for solving MCGM. In phase 1, for each dataset, multilocus ordering is performed combined with iterative jackknife resampling to evaluate the stability of marker orders. In this phase, the ordering problem is reduced to the well-known traveling salesperson problem (TSP). Namely, for each dataset, we look for order that gives minimum sum of recombination distances between adjacent markers. In phase 2, the optimal consensus order of shared markers is selected from the set of allowed orders and gives the minimal sum of total lengths of nonconflicting maps of the chromosome. This criterion may be used in different modifications to take into account the variation in quality of the original data (population size, marker quality, etc.). In the foregoing formulation, consensus mapping is considered as a specific version of TSP that can be referred to as “synchronized TSP.” The conflicts detected after phase 1 are resolved using either a heuristic algorithm over the entire chromosome or an exact/heuristic algorithm applied subsequently to the revealed small non-overlapping regions with conflicts separated by non-conflicting regions. The proposed approach was tested on a wide range of simulated data and real datasets from maize.
机译:对不同物种进行的许多制图项目已经产生了大量的制图数据。因此,对于同一生物,使用不同的作图种群和标记集构建了许多多基因座图。地图的质量在人群,标记集和使用的软件之间差异很大,因此需要努力整合地图信息并生成共识地图。与基于单个数据集的遗传图谱相比,共识遗传图谱(MCGM)的问题要困难得多。共有分析带来的其他并发症包括:群体间重组率差异和沿染色体的交换分布;所采用标记的优势变化;在不同的实验室中使用不同的标记子集。因此,有必要处理共享标记集的任意模式以及不同级别的映射数据质量。在本文中,我们介绍了一种解决MCGM的两阶段方法。在阶段1中,对于每个数据集,都执行多轨迹排序与迭代折刀重采样相结合以评估标记顺序的稳定性。在此阶段,将订购问题简化为众所周知的旅行销售员问题(TSP)。也就是说,对于每个数据集,我们寻找的顺序应使相邻标记之间的重组距离之和最小。在阶段2中,从允许顺序的集合中选择共享标记的最佳共有顺序,并给出染色体非冲突图谱总长度的最小总和。可以在不同的修改中使用此标准,以考虑原始数据质量的变化(种群大小,标记质量等)。在前面的表述中,共识映射被认为是TSP的特定版本,可以称为“同步TSP”。在阶段1之后检测到的冲突可以使用整个染色体上的启发式算法解决,也可以使用精确/启发式算法解决,然后将其应用到显示的较小的非重叠区域,并以非冲突区域分隔冲突。在广泛的模拟数据和玉米真实数据集上测试了该方法。

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