Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/29061
Title: Analytical validation of an error-corrected ultra-sensitive ctDNA next-generation sequencing assay.
Authors: Azad A.A.;Ng N.;Martelotto L.;Hauser C.;Southey M.C.;Nguyen-Dumont T.U.;Fettke H.;Steen J.A.;Kwan E.M.;Bukczynska P.;Keerthikumar S.;Goode D.;Docanto M.
Institution: (Fettke, Kwan, Docanto, Azad) Department of Medicine, School of Clinical Sciences, Monash University, Melbourne, Australia (Steen, Southey, Nguyen-Dumont) Precision Medicine, School of Clinical Sciences at Monash Health, Melbourne, Australia (Kwan) Department of Medical Oncology, Monash Health, Melbourne, Australia (Bukczynska, Martelotto, Hauser) Cancer Research Division, Peter MacCallum Cancer Centre, Melbourne, Australia (Keerthikumar, Goode) Computational Cancer Biology Program, Cancer Research Division, Peter MacCallum Cancer Centre, Melbourne, Australia (Keerthikumar, Goode, Azad) Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia (Ng) Walter & ElizaHall Institute of Medical Research, Melbourne, Australia (Southey, Nguyen-Dumont) Department of Clinical Pathology, University of Melbourne, Melbourne, Australia (Southey) Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Australia (Azad) Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia
Issue Date: 27-Oct-2020
Copyright year: 2020
Publisher: Future Science Ltd (E-mail: info@future-science.com)
Place of publication: United States
Publication information: BioTechniques. 69 (2) (pp 133-140), 2020. Date of Publication: 2020.
Journal: BioTechniques
Abstract: Plasma circulating tumor DNA (ctDNA) analysis has emerged as a minimally invasive means to perform molecular tumor typing. Here we developed a custom ultra-sensitive ctDNA next-generation sequencing assay using molecular barcoding technology and off-the-shelf reagents combined with bioinformatics tools for enhanced ctDNA analysis. Assay performance was assessed via a spike-in experiment and the technique was applied to analyze 41 plasma samples from men with advanced prostate cancer. Orthogonal validation was performed using a commercial assay. Sensitivity and specificity of 93 and 99.5% were recorded for ultra-rare somatic variants (<1%), with high concordance observed between the in-house and commercial assays. The optimized protocol dramatically improved the efficiency of the assay and enabled the detection of low-frequency somatic variants from plasma cell-free DNA (cfDNA).Copyright © 2020 Arun Azad.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.2144/BTN-2020-0045
PubMed URL: 32654508 [http://www.ncbi.nlm.nih.gov/pubmed/?term=32654508]
ISSN: 0736-6205
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/29061
Type: Article
Type of Clinical Study or Trial: Observational study (cohort, case-control, cross sectional or survey)
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