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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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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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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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