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I use abPOA to produce multiple consensus sequence, three most frequency sequences are
1 with a depth 25
CCCTCCCTTCCTTTCTTTCTCTCTTTCTCCCTCTCTTTCTCTTTCATTTTTCCTC
2 with a depth 40
CCCTTCCTTCCTTTCTTTCTCTCTTTCTCCCTCTCTTTCTCTTTCATTTTTCCTC
3 with a depth 23
CCCTCCCTTCCTTTCTTTCTCTCTTTCTCCCTCTCTTTCTCTTTCATTT
But the high depth allele "3" missing in the final consensus sequences ? I just curious how abPOA cluster the input sequence and whether I have taked some mistakes.
In the new version of your release, 3 or more cons are supported as mentioned.
In the GitHub, you have mentioned
The general underlying idea is to group input sequences into multiple clusters based on the heterozygous bases in the graph, Then, one consensus sequence is separately generated for each cluster of input sequences. The minimum allele frequency for each heterozygous base is 0.25.
But in my case, the third most common sequences are higher than this threshold.
Hi,
I use abPOA to produce multiple consensus sequence, three most frequency sequences are
But the high depth allele "3" missing in the final consensus sequences ? I just curious how abPOA cluster the input sequence and whether I have taked some mistakes.
The command I run is:
-d6 -m 0 -q 0.01 -a 0
The input fasta file is as below:
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