Center for Medical Ethics and Health Policy Staff Publications
Language
English
Publication Date
7-1-2022
Journal
Journal of Molecular Diagnostics
DOI
10.1016/j.jmoldx.2022.03.011
PMID
35487348
PMCID
PMC9302205
PubMedCentral® Posted Date
7-1-2022
PubMedCentral® Full Text Version
Post-print
Abstract
Somatic copy number alterations (SCNAs) in tumors are clinically significant diagnostic, prognostic, and predictive biomarkers. SCNA detection from targeted next-generation sequencing panels is increasingly common in clinical practice; however, detailed descriptions of optimization and validation of SCNA pipelines for small targeted panels are limited. This study describes the validation and implementation of a tumor-only SCNA pipeline using CNVkit, augmented with custom modules and optimized for clinical implementation by testing reference materials and clinical tumor samples with different classes of copy number variation (CNV; amplification, single copy loss, and biallelic loss). Using wet-bench and in silico methods, various parameters impacting CNV calling, including assay-intrinsic variables (establishment of normal reference and sequencing coverage), sample-intrinsic variables (tumor purity and sample quality), and CNV algorithm-intrinsic variables (bin size), were optimized. The pipeline was trained and tested on an optimization cohort and validated using an independent cohort with a sensitivity and specificity of 100% and 93%, respectively. Using custom modules, intragenic CNVs with breakpoints within tumor suppressor genes were uncovered. Using the validated pipeline, re-analysis of 28 pediatric solid tumors that had been previously profiled for mutations identified SCNAs in 86% (24/28) samples, with 46% (13/28) samples harboring findings of potential clinical relevance. Our report highlights the importance of rigorous establishment of performance characteristics of SCNA pipelines and presents a detailed validation framework for optimal SCNA detection in targeted sequencing panels.
Keywords
Algorithms, Child, DNA Copy Number Variations, High-Throughput Nucleotide Sequencing, Humans, Neoplasms, Sequence Analysis, DNA
Published Open-Access
yes
Recommended Citation
Chandramohan, Raghu; Reuther, Jacquelyn; Gandhi, Ilavarasi; et al., "A Validation Framework for Somatic Copy Number Detection in Targeted Sequencing Panels" (2022). Center for Medical Ethics and Health Policy Staff Publications. 146.
https://digitalcommons.library.tmc.edu/med_ethics/146