Lanner Julia, Curto Manuel, Pachinger Bärbel, Neumüller Ulrich, Meimberg Harald
a Institute for Integrative Nature Conservation Research , University of Natural Resources and Life Sciences , Vienna , Austria.
b Institute of Evolutionary Ecology and Conservation Genomics , University of Ulm , Ulm , Germany.
Mitochondrial DNA A DNA Mapp Seq Anal. 2019 Apr;30(3):490-499. doi: 10.1080/24701394.2018.1551386. Epub 2019 Jan 11.
DNA barcoding constitutes a supplemental genetically based characterization tool for the identification of species. Traditionally, the barcodes are generated with a length of 650 bp using standardized Sanger sequencing, but with the introduction of high-throughput sequencing (HTS) methods new opportunities for sequencing are available. To use HTS for barcode collection and identification, the amplification of shorter fragments is preferred. Reference DNA midi-barcodes of wild bees were produced using the Illumina MiSeq as well as the Sanger method. Although DNA midi-barcodes derived from Illumina were comparatively shorter (418 bp), their sequences were coherent to the morphological assignment of species. The Illumina barcodes proved to be effective and dealt better with some general limitations of DNA barcoding.
DNA条形码是一种基于基因的补充性物种鉴定工具。传统上,条形码是使用标准化的桑格测序法生成,长度为650 bp,但随着高通量测序(HTS)方法的引入,出现了新的测序机会。为了将HTS用于条形码收集和鉴定,更倾向于扩增较短的片段。使用Illumina MiSeq以及桑格法生成了野生蜜蜂的参考DNA中型条形码。尽管源自Illumina的DNA中型条形码相对较短(418 bp),但其序列与物种的形态学分类一致。Illumina条形码被证明是有效的,并且能更好地应对DNA条形码的一些普遍局限性。