Figure 1.

Overview of patient consent to treatment stratification workflow. Following patient consent, the tumour sample is assessed by a pathologist. This is then followed by DNA extraction and NGS sequencing. Bioinformatical data analysis is followed by data curation and validation of molecular targets.⁵ The resulting molecular alterations are then evaluated and reviewed at the GTAB meeting and treatment options for the patient determined. The outcome of the GTAB meeting is then reported to the relevant clinicians, the wider multidisciplinary team and the patient. Figure 1 was modified with permission from Horak et al.⁵