...
【24h】

Microcoding: the second step in DNA barcoding

机译:微编码:DNA条形码的第二步

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

After the process of DNA barcoding has become well advanced in a group of organisms, as it has in the economically important fungi, the question then arises as to whether shorter and literally more barcode-like DNA segments should be utilized to facilitate rapid identification and, where applicable, detection. Through appropriate software analysis of typical full-length barcodes (generally over 500 base pairs long), uniquely distinctive oligonucleotide 'microcodes' of less than 25 bp can be found that allow rapid identification of circa 100-200 species on various array-like platforms. Microarrays can in principle fulfill the function of microcode-based species identification but, because of their high cost and low level of reusability, they tend to be less cost-effective. Two alternative platforms in current use in fungal identification are reusable nylon-based macroarrays and the Luminex system of specific, colour-coded DNA detection beads analysed by means of a flow cytometer. When the most efficient means of rapid barcode-based species identification is sought, a choice can be made either for one of these methodologies or for basic high-throughput sequencing, depending on the strategic outlook of the investigator and on current costs. Arrays and functionally similar platforms may have a particular advantage when a biologically complex material such as soil or a human respiratory secretion sample is analysed to give a census of relevant species present.
机译:DNA条形码的编码过程已在一组生物中取得了很好的进展,就像它在经济上重要的真菌中一样,随后出现了一个问题,即是否应使用较短且字面上更多的条形码样DNA片段来促进快速识别,并且在适用的情况下进行检测。通过对典型的全长条形码(通常超过500个碱基对)进行适当的软件分析,可以发现小于25 bp的独特区别性寡核苷酸“微码”,可以在各种阵列状平台上快速鉴定大约100-200种。芯片原则上可以满足基于微码的物种识别的功能,但是由于成本高,可重用性低,它们的成本效益往往较低。当前在真菌鉴定中使用的两个替代平台是可重复使用的基于尼龙的宏阵列,以及通过流式细胞仪分析的特定颜色编码的DNA检测珠的Luminex系统。当寻求基于条形码的快速物种识别的最有效方法时,可以根据研究者的战略前景和当前成本,选择其中一种方法或基本的高通量测序。当分析生物复杂的材料(例如土壤或人类呼吸道分泌物样品)以对存在的相关物种进行普查时,阵列和功能相似的平台可能具有特殊优势。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号