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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
When sequencing PCR products, the fluorescent signal sometimes drops sharply and the PCR product sequence is not read completely. A typical cause of this problem is the presence of various inhibitors in templates of sequencing reactions.
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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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