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Description: Exome sequencing reaching a minimum depth of coverage of 100X. Sequencing comes with a full report on SNVs, INDELs and structural variants such as CNVs.
Genome sequencing reaching a minimum depth of coverage of 30X. Sequencing comes with a full report on SNVs, INDELs and structural variants such as CNVs. en
Description: Exome sequencing reaching a minimum depth of coverage of 100X. Sequencing comes with a full report on SNVs, INDELs and structural variants such as CNVs.