Fantastic!
solved my problems.
Thanks
Hi! I'm analyzing the results of few PCR product sequenced by Sanger method. I have the result using forward and reverse primer. Because the PCR products aren't too long, there are regions that overlaps, so I want to merge this to overlapping sequences to get only one big sequence.
Are there any online tool to do this?
Thanks!
The emboss package contains a tool named merger:
This joins two overlapping nucleic acid sequences into one merged sequence.
It uses a global alignment algorithm (Needleman & Wunsch) to optimally align the sequences and then it creates the merged sequence from the alignment. When there is a mismatch in the alignment between the two sequences, the correct base to include in the resulting sequence is chosen by using the base from the sequence which has the best local sequence quality score.
see also the related programs at the bottom of the page (cons and megamerger).
Fantastic!
solved my problems.
Thanks
I really like it because I can overlap more than 2 sequences. Thanks!
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Hi! I'm analyzing the results of around 400 PCR products sequenced by Sanger method. I have the result using forward and reverse primer. Because the PCR products aren't too long, there are regions that overlaps, so I want to merge this to overlapping sequences to get only one big sequence. I used primarily cap 3 but it not good, by DnaBaser I got some contig results but how can I join those sequences,,,,,
Are there any online tool to do this?
Thanks
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