Did you arrive here by selecting the   DNASTAR Navigator workflow Genomics > Resequencing and genotyping? If so, you’re in the right place!      

For exome, gene panel, cancer, or genome-wide association study (GWAS) studies, the following wizard selections are generally appropriate:

  • For cancer samples, check the box next to Somatic/Cancer/Heterogeneous in the Assembly Options screen.

In most cases, downstream analysis of the finished assembly will place in ArrayStar.

These two brief videos both demonstrate the reference-guided exome workflow:



The following video uses GWAS data. Note that the video shows an earlier version of the Choose Assembly Workflow screen with an option called Exome. In more recent versions of SeqMan NGen, this option is called Exome and gene panel.

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