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One of the biggest challenges facing us in this new age of genomic medicine is the functional validation of variants identified in exome/whole genome sequencing approaches. This article highlights the often difficult decisions we must face when confronted by a list of variants from genome-scale sequencing data and some key points to consider when deciding how to best test and validate, using animal models, any given variant as pathogenic.
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Timothy C. Cox (2015) studied this question.
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