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连锁分析法:一种利用新一代测序数据从单个二倍体个体中检测 SNP 和重建单体型的新方法。

The linkage method: a novel approach for SNP detection and haplotype reconstruction from a single diploid individual using next-generation sequence data.

机构信息

Graduate University for Advanced Studies, Hayama, Kanagawa, Japan.

出版信息

Mol Biol Evol. 2013 Sep;30(9):2187-96. doi: 10.1093/molbev/mst103. Epub 2013 May 31.

Abstract

When we sequence a diploid individual, the output actually comprises two genomes: one from the paternal parent and the other from the maternal parent. In this study, we introduce a novel heuristic algorithm for distinguishing single-nucleotide polymorphisms (SNPs) from the two parents and phasing them into haplotypes. The algorithm is unique because it simultaneously performs SNP calling and haplotype phasing. This approach can exploit the linkage information of nearby SNPs, which facilitates the efficient removal of haplotypes that originate from incorrectly mapped short reads. Using simulated data we demonstrated that our approach increased the accuracy of SNP calls. The haplotype reconstruction performance depended largely on the density of SNPs. Using current next-generation sequence technology with a relatively short read length, reasonable performance is expected when this approach is applied to species with an average of five heterozygous sites per 1 kb. The algorithm was implemented as the program "linkSNPs."

摘要

当我们对一个二倍体个体进行测序时,实际上会得到两个基因组:一个来自父本,另一个来自母本。在本研究中,我们引入了一种新颖的启发式算法,用于区分来自两个亲本的单核苷酸多态性(SNP)并将其相位成单倍型。该算法的独特之处在于它可以同时进行 SNP 调用和单倍型相位分析。这种方法可以利用附近 SNP 的连锁信息,有助于有效地去除源自错误映射短读的单倍型。使用模拟数据,我们证明了我们的方法提高了 SNP 调用的准确性。单倍型重构性能在很大程度上取决于 SNP 的密度。使用当前具有较短读长的下一代测序技术,当将该方法应用于平均每 1kb 有五个杂合位点的物种时,预计会有合理的性能。该算法已实现为程序“linkSNPs”。

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