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

Join our upcoming workshop or course!

NGS Data Analysis for Beginners | 3-Day In-Person Workshop

From the broader perspective, NGS data analysis is a two-step process only. First is quality control to get the best data set available. Second is the application-specific pipeline. This workshop will teach you to make the first step yourself. Its result will be a perfect mastery of NGS data quality control. 

16. - 18.4.2024 09:00 - 17:00 Prague, CZECH REPUBLIC Seats available: 14

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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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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

Some don't like it salty

One of the common problems with Sanger sequencing is samples with high salt concentration. In general, one could talk about inhibitors as such, but salts are probably the most common case. If you send us such samples, you will probably not be very…

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Is there a need for the reference gene(s) to be measured in the same plate (run) as the gene of interest?

In a relative quantification experiment, what you are most likely interested in is to compare the expression level of a particular gene among different samples. The most common way of correcting variations in the target nucleic acids input amount among…

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