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pgx_nat2_issue/cmds.sh

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# create the translation table after fixing the issue with the variant allele encoding
python /home/darren/Documents/2_repos/serenomica/pgx-engine/scripts/pharmvar_to_translation_table.py \
data/NAT2-6.2.15/GRCh38/NAT2.NC_000008.11.haplotypes.tsv \
"NAT2" \
"chr8"
# create the json (needed to change the saving location)
python /home/darren/Documents/2_repos/serenomica/pgx-engine/scripts/translation_to_json.py \
temp_NAT2_translation_table.tsv \
"NAT2" \
"chr8" \
"GRCh38" \
"NC_000008.11"