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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.
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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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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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