Unable to analyse this particular genome using official Docker container

Hi,

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I am using this command $ docker run -v "${pwd}:/app" genomicepidemiology/resfinder -ifa /app/input_genome.fasta -o test1_res_image -s "mycobacterium tuberculosis" --acquired --point

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I have tried in so many different ways to get this working with my genome (submitted to the resfinder server with ID 63C5582B000066E6751A2C21,although i accidently ran for Camplyobacter mutations), but it has not been working. It has been giving odd messages about keys (when a local installation is run). This only happens when looking for point mutations.

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Traceback (most recent call last):
  File "/miniconda3/envs/Isolate_seq/lib/python3.10/runpy.py", line 196, in _run_module_as_main
    return _run_code(code, main_globals, None,
  File "/miniconda3/envs/Isolate_seq/lib/python3.10/runpy.py", line 86, in _run_code
    exec(code, run_globals)
  File "/miniconda3/envs/Isolate_seq/lib/python3.10/site-packages/resfinder/__main__.py", line 5, in <module>
    sys.exit(main())
  File "/miniconda3/envs/Isolate_seq/lib/python3.10/site-packages/resfinder/run_resfinder.py", line 460, in main
    PointFinderResultHandler.standardize_results(std_result,
  File "/miniconda3/envs/Isolate_seq/lib/python3.10/site-packages/resfinder/cge/output/std_results.py", line 162, in standardize_results
    res_collection.add_class(cl="seq_regions", **gene_result)
  File "/miniconda3/envs/Isolate_seq/lib/python3.10/site-packages/cgelib/output/result.py", line 122, in add_class
    self._add_class_dict(cl, res, clobber, clobber_warn)
  File "/miniconda3/envs/Isolate_seq/lib/python3.10/site-packages/cgelib/output/result.py", line 130, in _add_class_dict
    val = self[cl].get(res["key"], None)
  File "/miniconda3/envs/Isolate_seq/lib/python3.10/collections/__init__.py", line 1106, in __getitem__
    raise KeyError(key)
KeyError: 'key'

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However, it works on this publicly available genome (just as a random example) . I am not sure if it is to do with a particular point mutation that occurs in some samples or not. https://www.ncbi.nlm.nih.gov/nuccore/NZ_MVHL01000001.1

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My assembly was from Nanopore reads, if that makes any difference.

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Any help on this would be much appreciated.

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