Target enrichment was performed using the SureSelect Clinical Research Exome v.2 and SureSelect Exome v.7 (Agilent). WES data processing, including sequence alignment to GRCh37 or GRCh38, and variant filtering and prioritization by allele frequency, predicted functional impact, and inheritance were...
Target enrichment was performed using the SureSelect Clinical Research Exome v.2 and SureSelect Exome v.7 (Agilent). WES data processing, including sequence alignment to GRCh37 or GRCh38, and variant filtering and prioritization by allele frequency, predicted functional impact, and inheritance were...
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