User: rucha.wadapurkar

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Posts by rucha.wadapurkar

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ClinVar database usage
... In ClinVar database,using variation viewer tool, after uploading .vcf file of identified mutations, all mutations are displaying in bottom resultant table, apart from those which are present in uploaded .vcf file. But I want to see only those mutations which are present in my .vcf file. How to do th ...
snp alignment next-gen sequence genome written 3 months ago by rucha.wadapurkar0

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