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.
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