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

Join our upcoming workshop or course!

Go Broad Before You Go Deep - Mastering NGS Technologies | 2-Day Online Course

For most, Next-Generation Sequencing equals to Illumina. This is a mistake! Staying on top of trends requires far broader view of the sequencing landscape. And this you will get in our course – we will not go deep, we will go broad! In just two days you will get full overview of NGS technologies and trust us, you would spend ages to do it yourself.

28. - 29.5.2024 09:00 - 16:30 Online Seats available: 27

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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 and reagents

Care of DNA sequencers and PCR cyclers, Sanger sequencing reagents.

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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

Combining Illumina and ONT reads makes your de novo assembly successful

Although state-of-the-art Next-Generation sequencing (NGS) technologies generate an adequate amount of sufficient quality data for de novo genome assembly of organisms for which the reference sequence is not known yet, the genome assembly process itself…

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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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