1. von Karsa L, Patnick J, Segnan N, Atkin W, Halloran S, Lansdorp-Vogelaar I, et al. European guidelines for quality assurance in colorectal cancer screening and diagnosis: overview and introduction to the full supplement publication. Endoscopy. 2013; 45:51–59.
Article
2. Kwon JH, Choi MG, Suh JP, Chang JH, Nam KW, Park HS, et al. The significance of fecal occult blood testing to screen for colon cancer. Korean J Gastrointest Endosc. 2007; 35:68–73.
3. Lim JU, Bae NY, Song WK, Cha JM, Lee JI. The significance of Fecal Immunochemical Test to Screen for Colorectal Cancer in National Cancer Screening Program. Intest Res. 2010; 8:126–134.
Article
4. Lamph S, Bennitt W, Brannon C, Halloran S. Evaluation report: immunochemical faecal occult blood tests. United Kingdom: National Health Service: Purchasing and Supply Agency;2009.
6. Jeon CH, Lee AJ, Kim KD. Annual report on external quality assessment scheme for urinalysis and faecal occult blood testing in Korea (2014). J Lab Med Qual Assur. 2015; 37:179–189.
Article
7. Allison JE. Colon Cancer Screening Guidelines 2005: the fecal occult blood test option has become a better FIT. Gastroenterology. 2005; 129:745–748.
Article
8. Allison JE, Tekawa IS, Ransom LJ, Adrain AL. A comparison of fecal occult-blood tests for colorectal-cancer screening. N Engl J Med. 1996; 334:155–159.
Article
9. Kim JH, Chung HJ, Yoon NS, Pyo YJ, Bae HG, Kim MN. Evaluation of the OC-SENSOR neo system for testing fecal occult blood. Korean J Lab Med. 2007; 27:210–215.
Article
10. Horiuchi Y, Masubuchi J, Oikawa S, Matsuda R, Hishinuma A, Ieiri T. Evaluation of fully automated fecal occult blood analyzer OC-SENSOR neo and OC-SENSOR II. Jap Assoc Clin Lab Auto. 2003; 28:40–46.
11. Okuyama Y, Doi Y, Matsuyama N, Uchino M, Yamamoto T. A novel sol particle immunoassay for fecal calprotectin in inflammatory bowel disease patients. Clin Chim Acta. 2016; 456:1–6.
Article
12. Tholen DW, Kallner A, Kennedy JW, Krouwer JS, Meier K. Evaluation of precision performance of quantitative measurement methods; approved guideline—second edition. CLSI document EP5-A2. Wayne, PA: Clinical and Laboratory Standards Institute;2004.
13. McEnroe R, Durham A, Goldford M, Kondratovich M, Lababidi S, Magari R, et al. Evaluation of precision of quantitative measurement procedures: approved guideline. CLSI document EP5-A3. Wayne, PA: Clinical and Laboratory Standards Institute;2014.
14. Daniel W, Martin K, Astles J. Evaluation of the linearity of quantitative measurement procedures: a statistical approach; approved guideline. CLSI document EP6-A2. Wayne, PA: Clinical and Laboratory Standards Institute;2003.
15. Krouwer JS, Cembrowski GS, Tholen DW. Preliminary evaluation of quantitative clinical laboratory measurement procedures; approved guideline. CLSI document EP10-A3. Wayne, PA: Clinical and Laboratory Standards Institute;2006.
16. Budd J, Durham A, Gwise T, Iriarte B, Kallner A, Linnet K, et al. Measurement procedure comparison and bias estimation using subject samples, approved quideline. CLSI document EP09-A3. Wayne, PA: Clinical and Laboratory Standards Institute;2013.
17. Hong SB, Kim HS, Park HS, Lee DH. Evaluation of the HM-JACK automatic analyzer for fecal occult blood test. J Lab Med Qual Assur. 2002; 24:221–224.
18. Kim DC, Cho SS, Song J, Kim EC, Kim JQ. Evaluation of the OC-SENSOR (Automatic Measuring Apparatus) for immunological fecal occult blood test. J Clin Pathol Qual Control. 1998; 20:281–287.
19. González AG, Herrador MÁ. A practical guide to analytical method validation, including measurement uncertainty and accuracy profiles. TrAC Trends in Analytical Chemistry. 2007; 26:227–238.
Article
20. Schiettecatte J, Anckaert E, Smitz J. Interferences in immunoassays. Adv Immunoass Technol. 2012.
Article