SNPWaveTM:: a flexible multiplexed SNP genotyping technology -: art. no. e47

被引:27
作者
van Eijk, MJT [1 ]
Broekhof, JLN [1 ]
van der Poel, HJA [1 ]
Hogers, RCJ [1 ]
Schneiders, H [1 ]
Kamerbeek, J [1 ]
Verstege, E [1 ]
van Aart, JW [1 ]
Geerlings, H [1 ]
Buntjer, JB [1 ]
van Oeveren, AJ [1 ]
Vos, P [1 ]
机构
[1] Keygene NV, NL-6700 AE Wageningen, Netherlands
关键词
D O I
10.1093/nar/gnh045
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Scalable multiplexed amplification technologies are needed for cost-effective large-scale genotyping of genetic markers such as single nucleotide polymorphisms (SNPs). We present SNPWave(TM), a novel SNP genotyping technology to detect various subsets of sequences in a flexible fashion in a fixed detection format. SNPWave is based on highly multiplexed ligation, followed by amplification of up to 20 ligated probes in a single PCR. Depending on the multiplexing level of the ligation reaction, the latter employs selective amplification using the amplified fragment length polymorphism (AFLP((R))) technology. Detection of SNPWave reaction products is based on size separation on a sequencing instrument with multiple fluorescence labels and short run times. The SNPWave technique is illustrated by a 100-plex genotyping assay for Arabidopsis, a 40-plex assay for tomato and a 10-plex assay for Caenorhabditis elegans, detected on the MegaBACE 1000 capillary sequencer.
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页数:13
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