免费的午餐:在现有扩增子面板中发现微单倍型改善了高度多态性的太平洋牡蛎的亲本分配。

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY G3: Genes|Genomes|Genetics Pub Date : 2025-02-05 DOI:10.1093/g3journal/jkae280
Neil F Thompson, Ben J G Sutherland, Timothy J Green, Thomas A Delomas
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引用次数: 0

摘要

通过测序方法使用基因分型的扩增子面板现在很常见,但主要集中在表征SNP标记。我们研究了在最近开发的太平洋牡蛎(Magallana gigas)扩增子面板中发现的微单倍型(MH)如何增加关系分配的统计能力。在一个592位点面板上对新建立的育种计划中三个种群的三胞胎(后代和两个亲本)进行了基因分型。处理后,92%的保留扩增子含有多态性MH变异,85%的单态SNP标记含有MH变异。等位基因丰富度的增加大大提高了关系分配的能力,大大降低了估计的假阳性率。SNP和MH数据集之间的分配准确性没有实质性差异,但使用MH增加了真父母和高度相关的潜在父母(阿姨和叔叔)之间对数似然值的分离。观察到大量的孟德尔不亲和性,可能是由于零等位基因。MH面板的进一步发展,包括去除具有高零等位基因率的位点,将通过减少面板大小来实现高通量基因分型,从而减少太平洋牡蛎研究和育种计划的成本。
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A free lunch: microhaplotype discovery in an existing amplicon panel improves parentage assignment for the highly polymorphic Pacific oyster.

Amplicon panels using genotyping by sequencing methods are now common, but have focused on characterizing SNP markers. We investigate how microhaplotype (MH) discovery within a recently developed Pacific oyster (Magallana gigas) amplicon panel could increase the statistical power for relationship assignment. Trios (offspring and two parents) from three populations in a newly established breeding program were genotyped on a 592 locus panel. After processing, 92% of retained amplicons contained polymorphic MH variants and 85% of monomorphic SNP markers contained MH variation. The increased allelic richness resulted in substantially improved power for relationship assignment with much lower estimated false positive rates. No substantive differences in assignment accuracy occurred between SNP and MH datasets, but using MHs increased the separation in log-likelihood values between true parents and highly related potential parents (aunts and uncles). A high number of Mendelian incompatibilities among trios were observed, likely due to null alleles. Further development of a MH panel, including removing loci with high rates of null alleles, would enable high-throughput genotyping by reducing panel size and therefore cost for Pacific oyster research and breeding programs.

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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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