The Disease Configuration section can be used to view, add, and edit the key genes associated with disease terms.
On the Configuration page, select the General tab.
Select Disease Configuration.
Select +New on the right side of the pane.
In the Disease Name field, type the disease name. This name can be based on a group of diseases or cancer types (for example, Bone).
In the Associated Disease Term(s) field, type a term (for example, Sarcoma).
Select the applicable term from the list that displays.
Make sure that the disease term displays under the field (for example, Sarcoma (SNOMEDCT: 1187396000)).
Under Key Genes, type a gene name in the field. You can enter one gene name per line, or multiple gene names separated by commas. A maximum of 250 names can be entered. The names are case-sensitive.
Select Save.
On the Configuration page, select the General tab.
Select Disease Configuration to expand the list of disease categories.
Select a disease (for example, Bone).
The following table shows the default key genes for select cancer types based on data provided by the Illumina Medical Affairs team.
The following resources can be used to identify other actionable genes to expand your key genes with:
On the Configuration page, select the General tab.
Select Disease Configuration.
Select ....
Update the disease terms as follows.
To add a disease term, type the term (for example, Sarcoma) in the Associated Disease Term(s) field.
Select the applicable term from the list that displays (e.g., Sarcoma (SNOMEDCT: 1187396000))
To delete a disease term, select the X next to it.
Select Save to accept any changes.
Update the key gene names as follows.
For Key Genes, enter a gene name in the field. You can enter one gene symbol per line, or multiple gene names separated by commas. A maximum of 250 names can be entered. The names are case-sensitive.
Select Save to accept any changes.
Update genome wide thresholds as follows.
For Genome Wide Thresholds, enter values for the following Tumor Mutational Burden (mut/MB) thresholds:
TMB-Low
TMB-High
Enter values for the following Microsatellite Instability thresholds, depending on the measurement used (i.e., % unstable sites or sumJSD):
MS-Stable
MSI-High
Enter values for the following Global Instability Score thresholds, depending on the algorithm used (i.e., Myriad or DRAGEN):
GIS-Low
GIS-High
Select Save to accept any changes.
Ovarian
BRCA1, BRCA2, FOXL2, NTRK1, NTRK2, NTRK3, ATM, BRIP1, MLH1, MSH2, PALB2, RAD51C, RAD51D, NBN, STK11
Colorectal
BRAF, ERBB2, KRAS, NRAS, NTRK1, NTRK2, NTRK3, MLH1, MSH2, MSH6, PMS2
CNS
ATRX, BRAF, EGFR, H3F3A, HIST1H3B, IDH1, IDH2, PTCH1, TERT, TP53, NTRK1, NTRK2, NTRK3, MGMT, PTEN
Bone
EWSR1, EGFR, ERG, ETV1, ETV4, FLI1, IDH1, NTRK1, NTRK2, NTRK3, FEV, IDH2, FUS
Other Solid (as a default for any other cancertypes)
ALK, APC, BCOR, BRAF, BRCA1, BRCA2, CDK4, CIC, CTNNB1, DNAJB1, ERBB2, EPCAM, ERG, ETV1, ETV4, ETV6, EWSR1, FGFR2, FGFR3, FOXO3, GLI1, IDH1, KIT, KRAS, MDM2, MLH1, MSH2, MSH6, MYOD1, NAB2, NTRK1, NTRK2, NTRK3, PAX3, PAX7, PDGFRA, PMS2, RANBP2, SDHB, SMARCB1, TFE3, WT1, YAP1, RET, ROS1, MET, IDH2
To confirm the action, select Yes,Restore to Default.
To confirm the action, select Yes, Delete.
Melanoma
BRAF, KIT, NRAS, NTRK1, NTRK2, NTRK3, TERT, GNAQ, GNA11, BAP1, SF3B1, EIF1AX, CDKN2A, BRCA2, PALB2, NF1, PTEN, CDK4, MC1R, MITF, MBD4
Prostate
ATM, BARD1, BRCA1, BRCA2, BRIP1, CDK12, CHEK2, FANCL, FGFR2, FGFR3, PALB2, PPP2R2A, RAD51B, RAD51C, RAD51D, RAD54L, NTRK1, NTRK2, NTRK3, ATR, EPCAM, ABRAXAS1, FANCA, GEN1, MLH1, MRE11, MSH2, MSH6, MUTYH, NBN, PMS2
Uterine and Cervical
ERBB2, ESR1, FOXO1, NCOA3, PAX3, PAX7, SMARCA4, SUZ12, NTRK1, NTRK2, NTRK3, ALK, ATRX, BCOR, CDK4, DICER1, FGFR2, GREB1, KMT2C, MDM2, MYBL1, NCOA2, CD274, PGR, PHF1, PIK3CA, PLAG1, RAD51B, RB1, TERT, TFE3, TP53, YWHAE, PTEN, POLE, MLH1, MSH2, MSH6, PMS2
Lung
ALK, BRAF, EGFR, ERBB2, KRAS, MET, NUTM1, RET, ROS1, NTRK1, NTRK2, NTRK3, CD274
Breast
BRCA1, BRCA2, ERBB2, ESR1, PIK3CA, NTRK1, NTRK2, NTRK3, CD274, PALB2, RAD51D, RAD51C, ATM, STK11, TP53, NF1, NBN, PTEN
Thyroid
BRAF, HRAS, KRAS, NRAS, RET, TERT, NTRK1, NTRK2, NTRK3, PAX8, PPARG, PTEN