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Updated: Dec 31, 2025

Infinium Assay for Large-scale SNP Genotyping Applications
Published on: November 19, 2013
An Axiom SNP genotyping array for Douglas-fir
Glenn T Howe1, Keith Jayawickrama2, Scott E Kolpak3
1Pacific Northwest Tree Improvement Research Cooperative, Department of Forest Ecosystems and Society, Oregon State University, Corvallis, OR, USA. glenn.howe@oregonstate.edu.
This study developed SNP assays for Douglas-fir, enabling large-scale genetic analysis for improved tree breeding and ecological studies. The new methods provide a foundation for population genomics and genomic selection in this important forest tree.
Area of Science:
- Forestry
- Genetics
- Plant Science
Background:
- Genetic markers are crucial for understanding forest tree populations, quantitative trait loci, gene function, and breeding.
- Advancements in genotyping technologies now allow for large-scale SNP analysis.
- Douglas-fir is a globally significant tree species economically and ecologically.
Purpose of the Study:
- To design and validate SNP assays for Douglas-fir (Pseudotsuga menziesii).
- To assess the utility of these SNPs for population genomics and genomic selection.
- To improve genome coverage and increase the number of reliably genotyped SNPs.
Main Methods:
- Designed SNP assays for over 55,000 potential SNPs based on transcriptome sequencing.
- Tested SNP assays on approximately 2,300 coastal and 13 interior Douglas-fir trees.
- Developed protocols to 'rescue' SNPs failing quality control by lowering call rate thresholds.
Main Results:
- As many as 28,000 SNPs were reliably genotyped and polymorphic.
- Lowering the SNP call rate threshold increased successful SNPs from 20,669 to 28,094.
- SNPs demonstrated good performance in Hardy-Weinberg equilibrium and minor allele frequency, and worked well on interior Douglas-fir.
Conclusions:
- The developed SNP assays can genotype 10,000-15,000 loci.
- The Axiom genotyping array provides a foundation for Douglas-fir population genomics and genomic selection.
- The array is currently being used to construct a linkage map and test genomic selection.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

