Hey i have detected mutations detected in both parents
how to identify mutations effecting child..& which are acting as carriers for disease.
Is thre any software to detect mutations for a given sequence data of both parents and child.
Do you have the child's genotype data? If so, you can use those de-novo mutation detection tools to do it
You could phase the variant calls (using GATK's PhaseByTransission) and pick variants with a specific inheritance pattern.
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