首页|基于SNP分子标记的新疆野生黄花苜蓿遗传多样性分析

基于SNP分子标记的新疆野生黄花苜蓿遗传多样性分析

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为揭示新疆野生黄花苜蓿的遗传多样性,研究利用SLAF-seq技术对材料进行SNP开发.结果显示,材料测序平均Q30值为96.32%,平均GC值为37.99%.研究共开发了 376 641个SLAF标签,多态性SLAF标签119 331个;SNP平均完整性为24.77%,平均杂合率5.53%.供试新疆野生黄花苜蓿品系的有效等位基因数、观测等位基因数、期望杂合度、观测杂合度和Shnnon Wiener指数的平均值分别为1.380、1.594、0.220、0.117和0.327.研究表明,聚类分析将材料分为7类,PCA将材料分为3类,但样品的来源为同一个祖先.
Genetic diversity analysis of wild Medicago falcata L.in Xinjiang based on SNP molecular markers
In order to reveal the genetic diversity of wild Medicago falcata L.in Xinjiang,SLAF-seq technology was used to develop SNP materials.The results showed that the average Q30 value and GC value were 96.32%and 37.99%,respectively.A total of 376 641 SLAF tags and 119 331 polymorphic SLAF tags were developed.The average integrity of SNP was 24.77%and the average heterozygosity was 5.53%.The average values of effective allele number,observed allele number,expected heterozygosity,observed heterozygosity,and Shnnon Wiener index were 1.380,1.594,0.220,0.117,and 0.327,respectively.The study indicates that cluster analysis divides the materials into seven categories,PCA divides the materials into three categories,but the samples come from the same ancestor.

Medicago falcata L.SLAF-seqmolecular markersgenetic diversitypopulation structure analysisphylogenetic relationship analysis

杜雨、于秀明、汪鹏、李倩、王玉祥、张博

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新疆农业大学草业学院,新疆乌鲁木齐 830052

黄花苜蓿 SLAF-seq 分子标记 遗传多样性 群体结构分析 亲缘关系分析

新疆维吾尔自治区重点研发任务专项新疆维吾尔自治区科技重大专项国家自然科学基金

2022B020032022A03004-131860675

2024

饲料研究
北京市营养源研究所

饲料研究

CSTPCD北大核心
影响因子:0.391
ISSN:1002-2813
年,卷(期):2024.47(4)
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