Symbol DNA

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

Join our upcoming workshop or course!

7th Prague Autumn School - RNASeq Data Analysis Workshop

We are again inviting you to join our data analysis workshop which covers all basic steps of Next-Generation sequencing data analysis. This five day computationally-intensive workshop focuses on quality control, sequence editing, read mapping and alignment. Additionally, this year we will pay a special attention to RNASeq data analysis. You will be briefly introduced into the Linux operating system and in this environment you will analyze sequencing data using various publicly available tools.

10. - 14.10.2022 09:00 - 17:00 Prague, CZECH REPUBLIC Seats available: 6

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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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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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A Few Thoughts on Troubleshooting of DNA Sequencing - Part III

Assuming we have good signals and read length is as expected which means we have successfully solved all issues mentioned in previous two parts of this post, we can still be far away from seeing nice data. This third part deals with the problem of having…

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