None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? Patients who have consented to the consent form for the subject and the consent form for human materials ? Patients over the age of 19 on the date of signing the consent form ? Patients who have the ability to make a written informed consent to voluntarily participate in this study ? Histologically confirmed advanced solid cancer patients (stage III or IV) ? Patients performing clinical targeted sequencing for diagnostic purposes during the treatment process
Exclusion criteria
Exclusion criteria: ? Patients who do not understand or do not consent to written consent ? Patients who do not have sufficient residual DNA of 500 ng or more after the clinical panel sequencing test ? Patients who do not consent to genetic testing
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| clinical validity of WGS in the patients who perfomed panel NGS | — |
Secondary
| Measure | Time frame |
|---|---|
| correlation between WGS and panel NGS | — |
Countries
Korea, Republic of
Contacts
Ajou University Hospital