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We are your reliable partner
in DNA sequencing
and Real-Time PCR

Join our upcoming workshop or course!

Next-Generation sequencing data analysis – Workshop for beginners

You will get acquainted with various formats of NGS data, you will learn about specific advantages and disadvantages of used sequencing technologies and how to deal with them, and you will understand the background of individual processes used to modify NGS data. After this three-day workshop, you will not become a bioinformatician, but you will be well on your way to becoming a qualified partner for bioinformaticians in your team.

7. - 9.6.2022 09:00 - 17:00 Warszawa, POLAND Seats available: 13

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Sanger sequencing and Fragment analysis

Sequencing of plasmids or PCR fragments, cleaning, special protocols.

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Next-generation sequencing

From project design to data analysis, high-throughput sequencing à la carte.

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Real-Time PCR

Courses and trainings, analysis of results. Are you planning Real-Time PCR experiments?

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Instrument Services

Care of Applied Biosystems® DNA sequencers and Real-Time PCR cyclers.

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Who we are

SEQme was established in 2012 to provide full solutions in DNA sequencing and Real-Time PCR.

We conduct sample analyses, organize courses and workshops focused on these techniques and provide instrument services.

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Our clients publish

Testimonials

Sample Collection Boxes

Use our sample collection boxes for sample shipment. These are regularly being serviced by our carrier service and the shipment is therefore free of charge!

Please make sure your samples are packed (in envelopes, for example) before placing them into the sample collection box.

Show box locations

SEQme Magazine

How do I sequence large templates directly?

Here and there we do receive a request to sequence large templates (i.e. chromosomal DNA, BACs, cosmids) directly. We can do this but similarly as for standard samples where short pcr products or plasmids serve as templates also here the key prerequisite…

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Sequencing of short PCR products

Sanger sequencing is associated with certain technical limitations, and one of the most important is read length. Typically, even with a perfectly flawless design, not more than a roughly 1,100 bases can be expected. But what is the lower limit of how…

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