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.
More about usYou 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.
Sequencing of plasmids or PCR fragments, cleaning, special protocols.
Tell me moreFrom project design to data analysis, high-throughput sequencing à la carte.
Tell me moreCourses and trainings, analysis of results. Are you planning Real-Time PCR experiments?
Tell me moreCare of Applied Biosystems® DNA sequencers and Real-Time PCR cyclers.
Tell me moreSEQme 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.
More about usUse 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 locationsHere 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…
READ MORERoutinely obtained sequence electropherograms typically start with unreliable (unreadable) data just at the beginning of a sequence. Although we should theoretically read the first base after the sequencing primer, there are often errors or truncations…
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