Using Sanger Sequencing

Understanding the relationship between genetic variation and biological function on a genomic scale is expected to provide fundamental new insights into the biology, evolution and pathophysiology of humans and other species The reason for the current enormous interest in SNPs is the hope that they could be used as markers to identify genes that predispose individuals to common, multifactorial disorders . If you need to genotype a low number of SNP´s in each of your samples (less than 15), than Sanger Sequencing is still the golden methodology that the customer should choose. Such small collection of SNPs occuring in genomic regions in which the frequencies of the SNP alleles differ between patients and controls. It is assumed that the SNP alleles are inherited together with the disease-predisposing alleles through the generations because they are physically close to each other. The disease-predisposing genes are genotyped in a fast and cost effective way.

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

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