Table 1.
Study characteristics | n | % |
---|---|---|
Province | ||
Ontario | 8 | 32 |
British Columbia | 8 | 32 |
Prairies (Alberta and Manitoba) | 4 | 16 |
Canada-Wide | 2 | 8 |
Quebec (alone or with USA) | 2 | 8 |
Maritimes (Nova Scotia) | 1 | 4 |
Study funding | ||
Public | 19 | 76 |
Not stated | 3 | 12 |
Private | 1 | 4 |
Public and private | 1 | 4 |
None | 1 | 4 |
Year of publication | ||
2016–2018 | 12 | 48 |
2013–2015 | 9 | 36 |
2010–2012 | 4 | 16 |
Clinical context | ||
Oncology | 15 | 60 |
Rare diseases | 5 | 20 |
Multiple/not specific | 3 | 12 |
Prenatal screening | 2 | 8 |
NGS technology | ||
NGS panels | 13 | 52 |
Oncotype DX | 6 | 24 |
WGS/WGTA | 5 | 20 |
Not specific | 4 | 16 |
WES and WGS | 2 | 8 |
WES | 1 | 4 |
Test strategy | ||
Prognosis | 10 | 40 |
Diagnosis | 9 | 36 |
Guide treatment | 3 | 12 |
Other/multiple | 3 | 12 |
WES, whole-exome sequencing; WGS/WGTA, whole-genome sequencing/whole-genome and transcriptome analysis, including cell-free DNA testing