Reads missing from alignment
Dear Philip
When aligning reads to a short reference, I saw that even small differences between the reference and the read caused a large drop in depth around the area of the divergence. This worries me, because the divergence is much lower that what I would expect would cause such a drop. Specifically, nucleotide identity is still above 85%, and there are stretches of more than 20 bases with 100% identity. BWA MEM finds the matches.
I’ve made a minimal working example, attached. Simply extract the archive and run the shell script.
Comments (10)
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reporter -
Dear Jakob
Which version of kma are you using, it worked with v1.3.19.
Best,
Philip -
reporter I was using KMA-1.3.10b. It’s working for me as well with v 1.3.19. Closing this issue
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reporter - changed status to resolved
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reporter - changed status to open
Unfortunately, it turned out it only solved the problem for the particular read in the minimal working example. Picking another read, it's still the same.
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reporter - attached files.tar.gz
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reporter @ptlcc I have updated the minimal example, such that it now also fails for the newest version of KMA
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Hi Jakob
I have found the bug, but it will take a little more to fix than usual. Fingers crossed en of this week, start of next at the latest.
Best,
Philip -
- changed status to resolved
Fixed Issue
#38→ <<cset 1f61d5a69d20>>
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Hi Jakob
It should be fixed now, v1.3.20.
Best,
Philip - Log in to comment
It seems like it works when setting
-mrs 0.1
. I don’t understand why that is, could it perhaps be better documented what-mrs X
does?X * length(read)
, since the alignment score for this read pair is around 150 for a 250 bp read.