Linda Amaral‐Zettler,Markus Bauer,Donna Berg-Lyons,Jason Betley,J. Greg Caporaso,Hugh W. Ducklow,Noah Fierer,Louise Fraser,Jack A. Gilbert,Niall Gormley,James S Huntley,Susan M. Huse,Janet Jansson,Simon Jarman,Rob Knight,Chris Lauber,Elizabeth A. McCliment,Sarah M. Owens,Geoff Smith,Luke Thompson,Hege Vestheim,William A. Walters
标识
DOI:10.17504/protocols.io.nuvdew6
摘要
The 18S protocol detailed here is designed to amplify eukaryotes broadly with a focus on microbial eukaryotic lineages. The primers target the 18S SSU rRNA and are based on those of Amaral-Zettler et al. (2009). The constructs are designed to be used with the Illumina platform. For running these libraries on the MiSeq and HiSeq, please make sure you read the supplementary methods of Caporaso et al. (2012). You will need to make your sample more complex by adding 5-10% PhiX to your run. The outlines of the protocol are the same as the 16S protocol, but different primers, PCR conditions, and sequencing primers are used. In addition, we have designed a blocking primer that reduces the amplification of vertebrate host DNA to be used on host-associated samples, especially those that have a low eukaryotic biomass. Blocking primer strategy is based on Vestheim et al. (2008).