Appendix Table A2.
Desiderata for the integration of whole genome studies into clinical decision support (CDS)
| CDS knowledge must have the potential to incorporate multiple genes and clinical information. |
| Keep CDS knowledge separate from variant classification. |
| CDS knowledge must have the capacity to support multiple EHR platforms with various data representations with minimal modification. |
| Support a large number of gene variants while simplifying the CDS knowledge to the extent possible. |
| Leverage current and developing CDS and genomics standards. |
| Support a CDS knowledge base deployed at and developed by multiple independent organizations. |
| Access and transmit only the genomic information necessary for CDS |
Reproduced with permission from Welch et al.8