How was the batch-specific supplementary NGS data produced and analysed?

The following reference standards are offered with batch-specific NGS data: HD848, HD846.

Each batch was sequenced using Agilent's CREV4 (Clinical Research Exome)  kit with a depth of 250x on Illumina platform. Raw reads are run through the Illumina DRAGEN Somatic Pipeline , which performs mapping, sorting and variant calling. The data has not been filtered.