Abstract
Application of single nucleotide polymorphisms (SNPs) is revolutionizing human bio-medical research. However, discovery of polymorphisms in low polymorphic species is still a challenging and costly endeavor, despite widespread availability of Sanger sequencing technology. We present CRoPS™ as a novel approach for polymorphism discovery by combining the power of reproducible genome complexity reduction of AFLP® with Genome Sequencer (GS) 20/GS FLX next-generation sequencing technology. With CRoPS, hundreds-of-thousands of sequence reads derived from complexity-reduced genome sequences of two or more samples are processed and mined for SNPs using a fully-automated bioinformatics pipeline. We show that over 75% of putative maize SNPs discovered using CRoPS are successfully converted to SNPWave® assays, confirming them to be true SNPs derived from unique (single-copy) genome sequences. By using CRoPS, polymorphism discovery will become affordable in organisms with high levels of repetitive DNA in the genome and/or low levels of polymorphism in the (breeding) germplasm without the need for prior sequence information. © 2007 van Orsouw et al.
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CITATION STYLE
van Orsouw, N. J., Hogers, R. C. J., Janssen, A., Yalcin, F., Snoeijers, S., Verstege, E., … van Eijk, M. J. T. (2007). Complexity reduction of polymorphic sequences (CRoPSTM): A novel approach for large-scale polymorphism discovery in complex genomes. PLoS ONE, 2(11). https://doi.org/10.1371/journal.pone.0001172
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