Daigle Derek, Simen Birgitte B, Pochart Pascale
454 Life Sciences, Branford, Connecticut, USA.
Curr Protoc Mol Biol. 2011 Oct;Chapter 7:Unit7.5. doi: 10.1002/0471142727.mb0705s96.
This unit describes a method to convert PCR products (amplicons) flanked by universal M13 primers into a library for use on all 454 Sequencing Systems (454 Life Sciences, a Roche Company). This is especially useful for simultaneous sequencing and analysis of large numbers of amplicons or for the detection of minor variations within the amplified products. The method described here involves preparing a library of DNA with specific primers containing adaptor sequences recognized by the GS Junior System sequencing process. The data from the sequencing run are processed and analyzed by 454 Life Sciences software. This approach allows for multiplexing of a large number of amplicons to streamline processing and analysis. Any pre-existing universally tagged amplicon, primer set, or plasmid with M13 sequences flanking the cloning site can be used in this protocol.
本单元介绍了一种方法,可将两侧带有通用M13引物的PCR产物(扩增子)转化为文库,用于所有454测序系统(454生命科学公司,罗氏公司旗下)。这对于同时对大量扩增子进行测序和分析,或检测扩增产物中的微小变异特别有用。这里描述的方法包括用含有被GS Junior系统测序过程识别的接头序列的特异性引物制备DNA文库。测序运行得到的数据由454生命科学公司的软件进行处理和分析。这种方法允许对大量扩增子进行多重分析,以简化处理和分析过程。任何预先存在的带有克隆位点两侧M13序列的通用标记扩增子、引物组或质粒均可用于本方案。