Integron_Finder
Integron_Finder copied to clipboard
[BUG] Wrong coordinates in results
Describe the bug Hi, First thanks for the nice work on this tool. I have been using this tool in a pipeline of mine and it has been working awesomely.
Recently I tried using it with some vibrio
genomes, and it has been showing problems with the annotation of integrons that happen in the very start of the sequences.
If many fails because it has sometimes generated results at the very first base and writing it as 0-index for example. And in some other, it has generated wrong negative start positions as below:
13 Integron_Finder integron 69515 74987 . + 1 ID=integron_01;integron_type=complete
24 Integron_Finder integron 25 12675 . + 1 ID=integron_01;integron_type=CALIN
25 Integron_Finder integron 19 9958 . + 1 ID=integron_01;integron_type=CALIN
27 Integron_Finder integron 6936 9536 . + 1 ID=integron_01;integron_type=complete
31 Integron_Finder integron 478 4564 . + 1 ID=integron_01;integron_type=CALIN
32 Integron_Finder integron 66 4604 . + 1 ID=integron_01;integron_type=CALIN
33 Integron_Finder integron 117 4047 . + 1 ID=integron_01;integron_type=CALIN
37 Integron_Finder integron -2 3108 . + 1 ID=integron_01;integron_type=CALIN
38 Integron_Finder integron 2 2804 . + 1 ID=integron_01;integron_type=CALIN
44 Integron_Finder integron 70 1709 . + 1 ID=integron_01;integron_type=CALIN
46 Integron_Finder integron -17 1603 . + 1 ID=integron_01;integron_type=CALIN
I am thus, sharing the gbk files that were generated by integron_finder
itself during analysis so that you can see the generated results, while at the same time having the contig sequence for reproducing it.
To Reproduce
integron_finder --local-max --func-annot --pdf --gbk --cpu 4 vibrio31.fna
Expected behavior
The minimum allowed starting base should be 1, not 0 nor negative.
OS:
- [X] Linux
- [ ] Windows
- [ ] Mac
Integron_Finder Version:
version 2.0.1