1 Willis J, "Validation of microsatellite instability detection using a comprehensive plasma-based genotyping panel" 25 : 7035-7045, 2019
2 Crysup B, "Using unique molecular identifiers to improve allele calling in low-template mixtures" 63 : 102807-, 2023
3 Jacobs MT, "Use of low-frequency driver mutations detected by cell-free circulating tumor DNA to guide targeted therapy in non-small-cell lung cancer : a multicenter case series" 2 : 1-10, 2018
4 Acuna-Hidalgo R, "Ultra-sensitive sequencing identifies high prevalence of clonal hematopoiesis-associated mutations throughout adult life" 101 : 50-64, 2017
5 Jamal-Hanjani M, "Tracking the evolution of non-small-cell lung cancer" 376 : 2109-2121, 2017
6 Bruehl FK, "Tiered somatic variant classification adoption has increased worldwide with some practice differences based on location and institutional setting" 146 : 822-832, 2022
7 Ponti G, "The value of fluorimetry(Qubit)and spectrophotometry(NanoDrop)in the quantification of cell-free DNA(cfDNA)in malignant melanoma and prostate cancer patients" 479 : 14-19, 2018
8 Henriksen TV, "The effect of surgical trauma on circulating free DNA levels in cancer patients-implications for studies of circulating tumor DNA" 14 : 1670-1679, 2020
9 Parpart-Li S, "The effect of preservative and temperature on the analysis of circulating tumor DNA" 23 : 2471-2477, 2017
10 Li Z, "The cornerstone of integrating circulating tumor DNA into cancer management" 1871 : 1-11, 2019
11 Tomczak K, "The Cancer Genome Atlas(TCGA) : an immeasurable source of knowledge" 19 : A68-A77, 2015
12 Horak P, "Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)" 24 : 986-998, 2022
13 Richards S, "Standards and guidelines for the interpretation of sequence variants : a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology" 17 : 405-424, 2015
14 Li MM, "Standards and guidelines for the interpretation and reporting of sequence variants in cancer: A joint consensus recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists" 19 : 4-23, 2017
15 Chakravarty D, "Somatic genomic testing in patients with metastatic or advanced cancer : ASCO provisional clinical opinion" 40 : 1231-1258, 2022
16 Sequence Variant Working Group, "Sequence Variant Interpretation"
17 Koessler T, "Reliability of liquid biopsy analysis : an inter-laboratory comparison of circulating tumor DNA extraction and sequencing with different platforms" 100 : 1475-1484, 2020
18 Heitzer E, "Recommendations for a practical implementation of circulating tumor DNA mutation testing in metastatic non-small-cell lung cancer" 7 : 100399-, 2022
19 Wang Q, "Real-time PCR evaluation of cell-free DNA subjected to various storage and shipping conditions" 14 : 12797-12804, 2015
20 Meddeb R, "Quantifying circulating cell-free DNA in humans" 9 : 5220-, 2019
21 van Ginkel JH, "Preanalytical blood sample workup for cell-free DNA analysis using Droplet Digital PCR for future molecular cancer diagnostics" 6 : 2297-2307, 2017
22 Li MM, "Points to consider for reporting of germline variation in patients undergoing tumor testing : a statement of the American College of Medical Genetics and Genomics(ACMG)" 22 : 1142-1148, 2020
23 Abbosh C, "Phylogenetic ctDNA analysis depicts early-stage lung cancer evolution" 545 : 446-451, 2017
24 Medina Diaz I, "Performance of Streck cfDNA blood collection tubes for liquid biopsy testing" 11 : e0166354-, 2016
25 "Performance evaluation guidelines for next generation sequencing in vitro diagnostic medical devices" Ministry of Food and Drug Safety
26 ICGC/TCGA Pan-Cancer of Whole Genomes Consortium, "Pan-cancer analysis of whole genomes" 578 : 82-93, 2020
27 Song Ho Hyun ; Park Hye Ran ; Cho Doohwan ; Bang Hae In ; 오혁진 ; Kim Jieun, "Optimization of a protocol for isolating cell-free DNA from cerebrospinal fluid" 2023
28 Chakravarty D, "OncoKB : a precision oncology knowledge base" 2017 : PO.17.00011-, 2017
29 Chakravarty D, "OncoKB : a precision oncology knowledge base" 2017 : 2017
30 "On-site inspection evaluation checklist"
31 Georgiadis A, "Noninvasive detection of microsatellite instability and high tumor mutation burden in cancer patients treated with PD-1 blockade" 25 : 7024-7034, 2019
32 Singh RR, "Next-generation sequencing in high-sensitive detection of mutations in tumors: challenges, advances, and applications" 22 : 994-1007, 2020
33 Parikh AR, "Minimal residual disease detection using a plasma-only circulating tumor DNA assay in patients with colorectal cancer" 27 : 5586-5594, 2021
34 Qiu P, "Measuring tumor mutational burden(TMB)in plasma from mCRPC patients using two commercial NGS assays" 9 : 114-, 2019
35 Kim SY, "Manual for guideline adaptation ver 2.0" National Evidence-based Healthcare Collaborating Agency 2011
36 Lee JS, "Liquid biopsy in pancreatic ductal adenocarcinoma : current status of circulating tumor cells and circulating tumor DNA" 13 : 1623-1650, 2019
37 Kloten V, "Liquid biopsy in colon cancer : comparison of different circulating DNA extraction systems following absolute quantification of KRAS mutations using Intplex allele-specific PCR" 8 : 86253-86263, 2017
38 "Laboratory accreditation program checklist, molecular diagnostic test"
39 Zheng Z, "Intratumor heterogeneity : A new perspective on colorectal cancer research" 9 : 7637-7645, 2020
40 Newman AM, "Integrated digital error suppression for improved detection of circulating tumor DNA" 34 : 547-555, 2016
41 Stout LA, "Identification of germline cancer predisposition variants during clinical ctDNA testing" 11 : 13624-, 2021
42 Bourbon E, "How to obtain a high quality ctDNA in lymphoma patients : preanalytical tips and tricks" 14 : 617-, 2021
43 Wang TT, "High efficiency error suppression for accurate detection of low-frequency variants" 47 : e87-, 2019
44 Jennings LJ, "Guidelines for validation of next-generation sequencing-based oncology panels : A joint consensus recommendation of the Association for Molecular Pathology and College of American Pathologists" 19 : 341-365, 2017
45 Meddeb R, "Guidelines for the preanalytical conditions for analyzing circulating cell-free DNA" 65 : 623-633, 2019
46 Cristiano S, "Genome-wide cell-free DNA fragmentation in patients with cancer" 570 : 385-389, 2019
47 Godsey JH, "Generic protocols for the analytical validation of next-generation sequencing-based ctDNA assays : a joint consensus recommendation of the BloodPAC’s Analytical Variables Working Group" 66 : 1156-1166, 2020
48 Trigg RM, "Factors that influence quality and yield of circulating-free DNA : a systematic review of the methodology literature" 4 : e00699-, 2018
49 Marcus L, "FDA approval summary : pembrolizumab for the treatment of tumor mutational burden-high solid tumors" 27 : 4685-4689, 2021
50 Stockley T, "Evidence-based best practices for EGFR T790M testing in lung cancer in Canada" 25 : 163-169, 2018
51 Diefenbach RJ, "Evaluation of commercial kits for purification of circulating free DNA" 228-9 : 21-27, 2018
52 Deveson IW, "Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology" 39 : 1115-1128, 2021
53 Mouliere F, "Enhanced detection of circulating tumor DNA by fragment size analysis" 10 : eaat4921-, 2018
54 Sozzi G, "Effects of prolonged storage of whole plasma or isolated plasma DNA on the results of circulating DNA quantification assays" 97 : 1848-1850, 2005
55 Chan KC, "Effects of preanalytical factors on the molecular size of cell-free DNA in blood" 51 : 781-784, 2005
56 Chiu RW, "Effects of blood-processing protocols on fetal and total DNA quantification in maternal plasma" 47 : 1607-1613, 2001
57 Abbosh C, "Early stage NSCLC – challenges to implementing ctDNA-based screening and MRD detection" 15 : 577-586, 2018
58 Pascual J, "ESMO recommendations on the use of circulating tumour DNA assays for patients with cancer : a report from the ESMO Precision Medicine Working Group" 33 : 750-768, 2022
59 Barra GB, "EDTA-mediated inhibition of DNases protects circulating cell-free DNA from ex vivo degradation in blood samples" 48 : 976-981, 2015
60 Jain M, "Direct comparison of QIAamp DSP Virus Kit and QIAamp Circulating Nucleic Acid Kit regarding cell-free fetal DNA isolation from maternal peripheral blood" 43 : 13-19, 2019
61 Schmitt MW, "Detection of ultra-rare mutations by next-generation sequencing" 109 : 14508-14513, 2012
62 Sundaresan TK, "Detection of T790M, the acquired resistance EGFR mutation, by tumor biopsy versus noninvasive blood-based analyses" 22 : 1103-1110, 2016
63 Kinde I, "Detection and quantification of rare mutations with massively parallel sequencing" 108 : 9530-9535, 2011
64 Moding EJ, "Detecting liquid remnants of solid tumors : circulating tumor DNA minimal residual disease" 11 : 2968-2986, 2021
65 Heitzer E, "Current and future perspectives of liquid biopsies in genomics-driven oncology" 20 : 71-88, 2019
66 조선미 ; Lee Hye Sun ; Jeon Soyoung ; Kim Yoonjung ; Kong Sun-Young ; Lee Jin Kyung ; Lee Kyung-A, "Cost-effectiveness analysis of three diagnostic strategies for the detection of EGFR mutation in advanced non-small cell lung cancer" 43 : 605-613, 2023
67 Bos MK, "Comparison of variant allele frequency and number of mutant molecules as units of measurement for circulating tumor DNA" 15 : 57-66, 2021
68 Bronkhorst AJ, "Comparison of methods for the isolation of cell-free DNA from cell culture supernatant" 42 : 1010428320916314-, 2020
69 Pérez-Barrios C, "Comparison of methods for circulating cell-free DNA isolation using blood from cancer patients : impact on biomarker testing" 5 : 665-672, 2016
70 Morgan SR, "Comparison of KRAS mutation assessment in tumor DNA and circulating free DNA in plasma and serum samples" 5 : 15-22, 2012
71 Genovese G, "Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence" 371 : 2477-2487, 2014
72 Shin Saeam ; Woo Hye In ; 김종원 ; M.D. Yoonjung Kim ; Lee Kyung-A, "Clinical practice guidelines for pre-analytical procedures of plasma epidermal growth factor receptor variant testing" 42 : 141-149, 2022
73 Larson KL, "Clinical outcomes of molecular tumor boards : a systematic review" 5 : 2021
74 Mouliere F, "Circulating tumor-derived DNA is shorter than somatic DNA in plasma" 112 : 3178-3179, 2015
75 Ignatiadis M, "Circulating tumor cells and circulating tumor DNA : challenges and opportunities on the path to clinical utility" 21 : 4786-4800, 2015
76 Merker JD, "Circulating tumor DNA analysis in patients with cancer : American Society of Clinical Oncology and College of American Pathologists joint review" 36 : 1631-1641, 2018
77 Azad TD, "Circulating tumor DNA analysis for detection of minimal residual disease after chemoradiotherapy for localized esophageal cancer" 158 : 494-505, 2020
78 Kamat AA, "Circulating cell-free DNA : a novel biomarker for response to therapy in ovarian carcinoma" 5 : 1369-1374, 2006
79 El Messaoudi S, "Circulating cell free DNA : preanalytical considerations" 424 : 222-230, 2013
80 Jung M, "Changes in concentration of DNA in serum and plasma during storage of blood samples" 49 : 1028-1029, 2003
81 Helman E, "Cell-free DNA next-generation sequencing prediction of response and resistance to third-generation EGFR inhibitor" 19 : 518-530, 2018
82 Gandara DR, "Blood-based tumor mutational burden as a predictor of clinical benefit in non-small-cell lung cancer patients treated with atezolizumab" 24 : 1441-1448, 2018
83 Clarke CA, "BLOODPAC : collaborating to chart a path towards blood-based screening for early cancer detection" 16 : 5-9, 2023
84 Ma X, "Analysis of error profiles in deep next-generation sequencing data" 20 : 50-, 2019
85 Pécuchet N, "Analysis of base-position error rate of next-generation sequencing to detect tumor mutations in circulating DNA" 62 : 1492-1503, 2016
86 Miller DT, "ACMG SF v3. 1 list for reporting of secondary findings in clinical exome and genome sequencing : A policy statement of the American College of Medical Genetics and Genomics(ACMG)" 24 : 1407-1414, 2022
87 Baker A, "A review of grading systems for evidence-based guidelines produced by medical specialties" 10 : 358-363, 2010
88 Wagner AH, "A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer" 52 : 448-457, 2020
89 Mateo J, "A framework to rank genomic alterations as targets for cancer precision medicine : the ESMO Scale for Clinical Actionability of molecular Targets(ESCAT)" 29 : 1895-1902, 2018
90 Sorber L, "A comparison of cell-free DNA isolation kits : isolation and quantification of cell-free DNA in plasma" 19 : 162-168, 2017
91 The Korean Society of Radiology, "2020 Clinical imaging guidelines for justification of diagnostic imaging study by types of patients"