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. 2019 Jul 5;13(5):467–476. doi: 10.1007/s12687-019-00428-5

Table 1.

Characteristics of included studies

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