Standardization of Sequencing Coverage Depth in NGS: Recommendation for Detection of Clonal and Subclonal Mutations in Cancer Diagnostics
Work
Year: 2019
Type: article
Abstract: The insufficient standardisation of diagnostic next-generation sequencing (NGS) still limits its implementation in clinical practice, with the correct detection of mutations at low variant allele freq... more
Source: Frontiers in Oncology
Authors Anna Petráčková, Michal Vašínek, Lenka Sedlaříková, Tereza Dýšková, Petra Schneiderová +3 more
Institutions University Hospital Olomouc, Palacký University Olomouc, VSB - Technical University of Ostrava
Cites: 20
Cited by: 106
Related to: 10
FWCI: 4.993
Citation percentile (by year/subfield): 99.99
Subfield: Cancer Research
Domain: Life Sciences
Sustainable Development Goal Partnerships for the goals
Open Access status: gold
APC paid (est): $2,950
Grant IDS MZ CR VES16-32339A, MH CZ — DRO (FNOl, 00098892)