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

The following reference standards are offered with batch-specific NGS data: HD848, HD846, HD867.

HD848 and 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. 

HD867:
Each batch was sequenced using Agilent's CREV4 (Clinical Research Exome) kit with a depth of 250x on Aviti platform. Raw reads are run through the Illumina DRAGEN Somatic Pipeline, which performs mapping, sorting and variant calling. The data has not been filtered.