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SEQme was established in 2012 to provide full solutions in the field of
DNA sequencing and Real-Time PCR.
We conduct sample analyses, organize courses and workshops
focused on these techniques and provide instrument services.
More about us
In the first part we discussed how to troubleshoot no or low signals. Basically empty electropherograms. Very frustrating. Now, I focus on another frequent result – you obtain some signals but the height of the DNA sequencing peaks diminished rapidly. A…
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Routinely 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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