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seqkit amplicon only keeps one amplicon #191
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Right, PCR could produce all combinations of the forward and backward primers. We should output them too. |
yeah exactly. In my case, the positions in the bed file would be enough. I would choose the amplicon I want and use the positions as trimming points for my fastq reads--but the sequences of the PCR products may be useful for other users. Thank you for considering it! |
Oh, you can use |
期待这个功能早日上线 |
Hi, I have the same issue here. Outputting the largest amplicon only was misleading in my case, as I was looking for an amplicon within repititive RNA genes of an eukaryotic genome. Instead of predicting a correct PCR amplicon of size around 400bp, As a solution, I see that outputting all valid amplicons is the best option, or you may add an option Here is a toy example
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Hi,
In version 0.15.0 seqkit amplicon only keeps one amplicon (the largest) per primer pair. I don't always care about the largest amplicon.
Would it be possible to implement the feature of keeping all valid amplicons? A bed file with the start and end bases (columns 2 and 3) of all valid pairs would be fantastic. That would permit me to inspect the amplicons and keep the one I want (in my case, the smallest amplicon over a certain threshold).
Thanks
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