Genome-wide association studies (GWAS) map genetic variants associated with diseases across the genome. GWAS typically focus on associations between single-nucleotide polymorphisms (SNPs) and traits like major diseases in humans or breeding traits in animals and plants.
Our GWAS support for:
Illumina SNP arrays
We offer assistance for both study design as well as further data analysis and interpretation with Illumina´s Infinium BeadChip, Omni Array family (SNP and CNV detection, whole-genome genotyping) which allow to genotype 50,000 to 5 million SNP markers per array.