Using Next-Gen Sequencing

Large-scale analysis of single nucleotide polymorphisms (SNPs) allow genes that underlie complex disease to be identified. STAB VIDA offers genotyping methods that are high throughput, accurate and cheap for gaining full access to the abundant genetic variation of organisms. Whole genome approaches using single nucleotide polymorphism (SNP) markers have the potential to transform complex disease genetics and expedite pharmacogenetics research. Our current technology platforms are able to deliver throughputs in excess of 100 000 genotypes per day, with an accuracy of >99%, at a cost of 20–30 cents per genotype. DNA template requirements are minimised such that hundreds of thousands of SNPs can be interrogated using a relatively small amount of genomic DNA.

Ongoing promotions

- Project with more than 200 samples for more than 20 SNP´s have a discount of 25% off this price list
- Run more than 50 samples for microsatellites and get discount plus 200 Base Equivalents of oligos

Find the pathways to disease from genotyping data
Tell us about your project and we will try our best to help
The best genotyping services
Genotype your chromosomes @ your easy genetics laboratory
What do your genes tell?
Genotype your samples @ your easy genetics laboratory

Ask for a Genotyping Quotation

Tell us more about your specific project needs, and we will be happy to send you a quotation. You can also request the visit of our Genotyping core facility manager for a discussion of the best approach to your research. Please click here or contact us by phone to the (+351) 212956721