html5 templates


double digest RAD Sequencing (ddRAD-Seq)

double digest RAD Sequencing (ddRAD-Seq) involves digesting a target genome with two restriction nucleases to efficiently identify and score genetic variants across any genome. With ddRAD-Seq, development of hundreds to tens of thousands of genetic markers can be accomplished quickly and effectively.

BioXplore offer a wide range of Services for ddRAD-Seq routinely used for a range of molecular genetic applications 

  • Identification of genetic variants (SNPs)
  • Linkage and QTL mapping
  • Population genetics
  • Marker-trait association


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.