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  • Genotyping companies in Denmark/EU

    What is the cheapest way of identifying known variants (SNPS, indels) ?

    I am currently based in Copenhagen and am involved with a start up.I have asked a commercial lab sequencing company for advice and they have mentioned either sanger sequencing or genotyping.But the prices for both seem a bit high.

    We would be identifying variants in atleast 10-15 genes so a panel might be an option as well.

  • #2
    It really depends on the number of samples and what kind of data you would like, there is no solution to fit all needs. Traditionally PCR-based genotyping (e.g. TaqMan) was the cheapest (at least for low number of target variants), but multiplexed amplicon sequencing with an NGS platform can be very cheap per datapoint these days. And you get a lot more context data "for free" (which you might not want to deal with).

    PM me if you need a technical contact at our company to discuss different possibilities in detail.
    Last edited by sarvidsson; 02-10-2015, 06:47 AM.

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