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Use of NGS to identify the causal variant associated with a complex phenotype

Use of NGS to identify the causal variant associated with a complex phenotype. Overview. Why are we sequencing? How did we select the animals to sequence? What are the steps involved in the process? What do you do with the reads once you have them? Where are we now?. Introduction.

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Use of NGS to identify the causal variant associated with a complex phenotype