New rapid and inexpensive SNP service available

Per O. Ekstrøm, Eivind Hovig and coworkers now announce the availability of a rapid and very inexpensive screening facility for selected single nucleotide polymorphisms (SNPs).

This service is especially useful for projects where there is a need to screen a relatively large amounts of individuals for selected SNPs (or pools of individuals).

Researchers who quickly need to check for a given allele variant for instance for a tumor-related gene or a drug-metabolizing gene in a number of patients or samples are encouraged to contact the group.

Click here to read more about the screening facility! (from Eivind Hovig's home page)