How to get a VCF file for all variants in a specific gene and specific exon?
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6.2 years ago

How to get a VCF file for all variants (single nucleotide variants, insertions/deletions, copy number variants and structural variants) from reference genome (e.g. GRCh38) for a specific gene (e.g. BRCA1) and in specific exon (e.g. 10) ?

Thanks.

SNP VCF BED • 1.6k views
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3.1 years ago
DNAngel ▴ 240

Have you figured this out? I am also interested!

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