首页> 美国卫生研究院文献>Ecology and Evolution >What remains from a 454 run: estimation of success rates of microsatellite loci development in selected newt species (Calotriton asper Lissotriton helveticus and Triturus cristatus) and comparison with Illumina-based approaches
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What remains from a 454 run: estimation of success rates of microsatellite loci development in selected newt species (Calotriton asper Lissotriton helveticus and Triturus cristatus) and comparison with Illumina-based approaches

机译:454运行的结果:估算选定selected物种(Calotriton asperLissotriton helveticus和Triturus cristatus)中微卫星基因座发育的成功率并与基于Illumina的方法进行比较

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摘要

The development of microsatellite loci has become more efficient using next-generation sequencing (NGS) approaches, and many studies imply that the amount of applicable loci is large. However, few studies have sought to quantify the number of loci that are retained for use out of the thousands of sequence reads initially obtained. We analyzed the success rate of microsatellite loci development for three amphibian species using a 454 NGS approach on tetra-nucleotide motif-enriched species-specific libraries. The number of sequence reads obtained differed strongly between species and ranged from 19,562 for Triturus cristatus to 55,626 for Lissotriton helveticus, with 52,075 reads obtained for Calotriton asper. PHOBOS was used to identify sequences with tetra-nucleotide repeat motifs with a minimum repeat number of ten and high quality primer binding sites. Of 107 sequences for T. cristatus, 316 for C. asper and 319 for L. helveticus, we tested the amplification success, polymorphism, and degree of heterozygosity for 41 primer combinations each for C. asper and T. cristatus, and 22 for L. helveticus. We found 11 polymorphic loci for T. cristatus, 20 loci for C. asper, and 15 loci for L. helveticus. Extrapolated, the number of potentially amplifiable loci (PALs) resulted in estimated species-specific success rates of 0.15% (T. cristatus), 0.30% (C. asper), and 0.39% (L. helveticus). Compared with representative Illumina NGS approaches, our applied 454-sequencing approach on specifically enriched sublibraries proved to be quite competitive in terms of success rates and number of finally applicable loci.
机译:使用下一代测序(NGS)方法,微卫星基因座的开发变得更加有效,许多研究表明适用的基因座数量很大。但是,很少有研究试图从最初获得的数千个序列读数中量化保留供使用的基因座数量。我们在富含四核苷酸基序的物种特异性文库中使用454 NGS方法分析了三个两栖物种的微卫星基因座开发成功率。物种之间获得的序列读数数量差异很大,范围从Triturus cristatus的19,562到Lissotriton helveticus的55,526,而Calotriton asper的获得的52,075读数。 PHOBOS用于鉴定具有四核苷酸重复基序的序列,其最小重复数为十,且引物结合位点质量较高。在107个T. cristatus序列,316个C. asper序列和319个L. helveticus序列中,我们测试了41个引物组合的扩增成功,多态性和杂合度,每个序列分别用于C. asper和T. cristatus,以及22个L. helveticus。我们找到了11个多态性位点,为T. cristatus,20个位点为C. asper和15个位点为L. helveticus。外推,潜在可扩增基因座(PAL)的数量导致估计的物种特异性成功率为0.15%(C. cristatus),0.30%(C. asper)和0.39%(L. helveticus)。与代表性的Illumina NGS方法相比,我们在特异富集子库上应用454测序方法在成功率和最终可应用基因座数量方面证明具有相当的竞争力。

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