Comments (1)
Suggest you turn a catalogue into three catalogues
Part A: nucleotide matches
Use VCF definition of catalogue, and match Drprg vcf with catalogue vcf. Some trickiness with indel normalisation.
Part B: amino variants
First translate the pandora-inferred sequence into amino sequence
Then,
- catalogue has two dictionaries. Both have key which is amino position /index in the reference amino sequence. First dictionary has value which is array of amino acids which cause resistance. Second dictionary has value which is array of amino acids which definitely don't cause resistance. WHO and others starting to provide these "definitely not a resistance variant" lists, could be useful to report.
Finally notice if there is
- stop codon
- Part of the Pandora sequence has zero coverage, signifying truncated gene
Part C
- rule about whether frameshifts or stop codon or truncations in a gene are meant to cause resistance. Frameshift detection by aligning amino sequence seems most reliable as you incorporate all variants at the same time. Otherwise you have multiple nucleotide positions nearby affecting the same codon
from drprg.
Related Issues (20)
- Run drprg HOT 4
- Add grammar for specifying variant "expert" rules
- Benchmark figures HOT 7
- Parse pandora VCF to detect minor alleles HOT 46
- Update pandora and make_prg HOT 2
- Deal with gene absence HOT 9
- Add some common resistance-conferring mutations that do no exist in population graph HOT 8
- Notice partial gene deletion that spans start codon HOT 8
- Targeted sequencing mode HOT 1
- Disruptive in-frame indels HOT 3
- Lineage calling HOT 1
- Add install instructions to README.md
- How do i pronounce this tool name HOT 1
- Installation_error HOT 2
- Collate_drprg_results HOT 1
- error: unrecognized subcommand 'index' HOT 4
- Paired-end fastq files HOT 1
- Missing expected output file /test/outdir/discover/denovo_sequences.fa HOT 5
- Index is not valid, missing files error HOT 2
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