Our microarray-based SNP genotyping services comprise of GeneChiP Axiom amd Illumina SNP arrays which allows powerful genome-wide association studies (GWAS) and can accurately detect point mutations and copy number variants
PMRA includes a genome-wide imputation grid with about 900,000 markers driving deeper scientific insights into a variety of important health questions related to common and rare inherited diseases, genetic risk profiling, immune response, pharmacogenomics research, and many other areas associated with precision medicine.
PMDA is a comprehensive imputation-aware genotyping resource designed to drive deeper scientific insights into complex disease susceptibility, pharmacogenomics (PGx), and genetic factors underlying wellness and lifestyle in diverse populations to advance population genomics studies.
It offers >850,000 markers selected for high genomic coverage from the 1000Genomes Project Phase III.
BeadChip is a next-generation genotyping array with about approx. 654,027 markers for population-scale genetics, variant screening, pharmacogenomics studies, and precision medicine research.
Knowledge on draft assemblies and genetic heterogeneity such as SNPs enabled the design of whole-genome SNP chips which are increasingly used to map quantitative trait loci (QTLs) as well as loci associated with increased resistance to common diseases of Livestock.
BioXplore offers the following Illumina´s Infinium BeadChips for Livestock animals like Bovine SNP50, Bovine HD, Porcine SNP60, Ovine SNP50, Equine SNP50, Canine SNP20 and Canine HD.