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My existing Gemini pipeline is based on GRCh37, and I want that to be
almost 100% compatible when I port to GRCh38. As part of the provenance
requirements of my environment, gemini's ability to bundle gene annotations
with variants is essential for me.
To be fully compatible with Gemini, is there any way for us to include the gene_summary and gene_detailed tables in the DB output as well?
One suggestion would be porting arq5x/gemini/gemini/gene_table.py to vcf2db, while allowing GTF file input from user.
Thanks a lot.
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