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What is the recommended workflow to produce a VCF file when starting with two unaligned bacterial whole-genome fasta files, each approximately 3 million nucleotides? Any particular aligner and file format conversion utilities you can recommend?
The text was updated successfully, but these errors were encountered:
What is the recommended workflow to produce a VCF file when starting with two unaligned bacterial whole-genome fasta files, each approximately 3 million nucleotides? Any particular aligner and file format conversion utilities you can recommend?
The text was updated successfully, but these errors were encountered: