PlexSeq™
Advanced, Accurate , Streamlined Genotyping
Our PlexSeq™ Platform bridges the gap between single-plex SNP assays and high-density arrays by providing next-generation sequencing analysis of your SNPs of interest.
PlexSeq™ is an amplicon-based sequencing method for assaying 25 to 5000 SNPs. With our methodology, you can simultaneously genotype all SNPs across thousands of samples.
Our innovative PlexCall™ software then analyzes the allele frequency and compiles your SNP calls into a concise report. The multiplex capabilities and streamlined genotype calling of PlexSeq™ provide data at a much lower cost and in less time than other platforms.
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Research and Breeding Applications
1
Quantitative Trait Loci (QTL) analysis and genetic mapping:
Genotype markers throughout the genome of parental lines and progeny to identify and map QTLs for your desired traits.
2
Trait Profiling
Create your own panel of trait-associated markers and profit from our ability to assay an unlimited number of samples to screen any germplasm for your traits of interest.
3
Marker-Assisted Selection, genomic selection, and backcrossing:
Simultaneously genotype background markers together with your trait markers to accurately estimate background recovery and recapture valuable genes from the recipient line.
Seed Quality Assurance Applications
1
Genetic Purity
Test for outcrossing, seed mixes, or seed swaps.
2
Trait confirmation and/or Adventitious Presence (AP) Testing
Confirm the presence of your transgenic traits, or search for adulteration of conventional seed by the Adventitious Presence (AP) of GM seed.
3
Varietal ID
Confirm or test the genetic makeup of your lines. There is no need to settle on panels of small numbers of DNA markers; with PlexSeq™, you can use multiple markers for higher resolution of closely related germplasm.