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直接叶绿体测序:用于全叶绿体条形码的测序平台与分析工具的比较

Direct chloroplast sequencing: comparison of sequencing platforms and analysis tools for whole chloroplast barcoding.

作者信息

Brozynska Marta, Furtado Agnelo, Henry Robert James

机构信息

Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, Brisbane, Queensland, Australia.

出版信息

PLoS One. 2014 Oct 17;9(10):e110387. doi: 10.1371/journal.pone.0110387. eCollection 2014.

Abstract

Direct sequencing of total plant DNA using next generation sequencing technologies generates a whole chloroplast genome sequence that has the potential to provide a barcode for use in plant and food identification. Advances in DNA sequencing platforms may make this an attractive approach for routine plant identification. The HiSeq (Illumina) and Ion Torrent (Life Technology) sequencing platforms were used to sequence total DNA from rice to identify polymorphisms in the whole chloroplast genome sequence of a wild rice plant relative to cultivated rice (cv. Nipponbare). Consensus chloroplast sequences were produced by mapping sequence reads to the reference rice chloroplast genome or by de novo assembly and mapping of the resulting contigs to the reference sequence. A total of 122 polymorphisms (SNPs and indels) between the wild and cultivated rice chloroplasts were predicted by these different sequencing and analysis methods. Of these, a total of 102 polymorphisms including 90 SNPs were predicted by both platforms. Indels were more variable with different sequencing methods, with almost all discrepancies found in homopolymers. The Ion Torrent platform gave no apparent false SNP but was less reliable for indels. The methods should be suitable for routine barcoding using appropriate combinations of sequencing platform and data analysis.

摘要

利用新一代测序技术对植物总DNA进行直接测序,可生成完整的叶绿体基因组序列,该序列有可能为植物和食品鉴定提供条形码。DNA测序平台的进展可能使这成为常规植物鉴定的一种有吸引力的方法。使用HiSeq(Illumina)和Ion Torrent(Life Technology)测序平台对水稻的总DNA进行测序,以鉴定野生稻植株相对于栽培稻(品种日本晴)的整个叶绿体基因组序列中的多态性。通过将序列读数映射到参考水稻叶绿体基因组,或通过从头组装并将所得重叠群映射到参考序列,生成了一致的叶绿体序列。通过这些不同的测序和分析方法,预测野生稻和栽培稻叶绿体之间共有122个多态性(单核苷酸多态性和插入缺失)。其中,两个平台均预测到总共102个多态性,包括90个单核苷酸多态性。不同测序方法下插入缺失的变异性更大,几乎所有差异都出现在同聚物中。Ion Torrent平台未出现明显的假单核苷酸多态性,但插入缺失的可靠性较低。这些方法通过测序平台和数据分析的适当组合,应适用于常规条形码分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dc2/4201551/2fbd54e73efa/pone.0110387.g001.jpg

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