دورية أكاديمية

A comprehensive next generation sequencing tissue assay for Asian-prevalent cancers—Analytical validation and performance evaluation with clinical samples

التفاصيل البيبلوغرافية
العنوان: A comprehensive next generation sequencing tissue assay for Asian-prevalent cancers—Analytical validation and performance evaluation with clinical samples
المؤلفون: Cedric Chuan-Young Ng, Sandy Lim, Abner Herbert Lim, Nur Diyana Md Nasir, Jingxian Zhang, Vikneswari Rajasegaran, Jing Yi Lee, Jessica Sook Ting Kok, Aye Aye Thike, Johnathan Xiande Lim, Ruifen Weng, Sidney Yee, Yukti Choudhury, Jason Yongsheng Chan, Puay Hoon Tan, Min-Han Tan, Bin Tean Teh
المصدر: Frontiers in Molecular Biosciences, Vol 9 (2022)
بيانات النشر: Frontiers Media S.A., 2022.
سنة النشر: 2022
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: next-generation sequence (NGS), hybrid capture, molecular diagnostics, asian cancers, genetic alteration, tissue assay, Biology (General), QH301-705.5
الوصف: Introduction: A well-validated diagnostic assay with curated biomarkers complements clinicopathological factors to facilitate early diagnosis and ensure timely treatment delivery. This study focuses on an Asian-centric cancer diagnostic assay designed and thoroughly validated against commercially available standard references and a cohort of over 200 clinical specimens spanning 12 diverse Asian-centric cancer types.Methods: The assay uses hybrid-capture probes capable of profiling DNA aberrations from 572 cancer-related genes and 91 RNA fusion partners. The panel can detect clinically-tractable biomarkers such as microsatellite instability (MSI) and tumor mutation burden (TMB).Results: Analytical evaluation demonstrated 100% specificity and 99.9% sensitivity within a ≥5% VAF limit of detection (LoD) for SNV/Indels. RNA-based fusion features an LoD of ≥5 copies per nanogram input when evaluated against commercial references. Excellent linearity and concordance were observed when benchmarking against orthogonal methods in identifying MSI status, TMB scores and RNA fusions. Actionable genetic alterations were identified in 65% of the clinical samples.Conclusion: These results demonstrate a molecular diagnostic assay that accurately detects genomic alterations and complex biomarkers. The data also supports an excellent performance of this assay for making critical diagnoses and well-informed therapeutic decisions in Asian prevalent cancers.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2296-889X
Relation: https://www.frontiersin.org/articles/10.3389/fmolb.2022.963243/full; https://doaj.org/toc/2296-889X
DOI: 10.3389/fmolb.2022.963243
URL الوصول: https://doaj.org/article/01db8eb942f6482085e4d3ecfd293907
رقم الأكسشن: edsdoj.01db8eb942f6482085e4d3ecfd293907
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2296889X
DOI:10.3389/fmolb.2022.963243