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how to add a column summarizing in which samples the variant was identified
priozization genotypes csv variants
2.7 years ago by Adham • 0
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Extract svtype from svaba
SV VCF SVTYPE SVABA
2.8 years ago by Adham • 0
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Functional annotation with VEP: combine the same variant between the samples in the same line (question)
output VEP Annotation
updated 2.9 years ago by ▴ 10 • written 3.0 years ago by • 0
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Comment: Comment: Construction of the reference genome database (GCA_000001405.15_GRCh38) with snp
3.1 years ago by Adham • 0
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Construction of the reference genome database (GCA_000001405.15_GRCh38) with snpeff
reference snpeff genome alignement annotation
updated 3.1 years ago by ★ 3.8k • written 3.1 years ago by • 0
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Question: Reference genome between variant calling and annotation with snpeff
snpeff calling hg38 variant grch38
3.1 years ago by Adham • 0
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