and ANNOVAR
and SeattleSeq Annotation
both for annotation of SNP variants. ie. Nonsense, synonymous, splice, intronic, found in 1000 genomes, or HapMap frequency, which gene, amino acid change (from and too, with position) etc.
and SeattleSeq Annotation
both for annotation of SNP variants. ie. Nonsense, synonymous, splice, intronic, found in 1000 genomes, or HapMap frequency, which gene, amino acid change (from and too, with position) etc.
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