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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 - Introduction

The aim of the course is to help you gain a basic orientation in technologies, principles, concepts and possibilities of using Next-Generation sequencing (NGS). Emphasis is placed on mastering the ability of independent effective planning of NGS experiments and basic evaluation of results. We will discuss the whole topic comprehensively from A to Z in context.

21. - 22.9.2020 09:00 - 17:00 Brno, CZECH REPUBLIC Seats available: 5
23. - 24.11.2020 09:00 - 17:00 Warsaw, POLAND Seats available: 17

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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 of 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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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

A Few Thoughts on Troubleshooting of DNA Sequencing - Part I

It is not the aim of this post to provide a detailed description of all problems you may observe when evaluating your sequencing results. Instead, I focus on most frequent problems and recommend some steps to take for your consideration. Additionally, I…

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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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