2021
DOI: 10.1016/j.pmpp.2021.101622
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Quantitative detection of pathogen load of Fusarium oxysporum f.sp. ciceris infected wilt resistant and susceptible genotypes of chickpea using intergenic spacer region-based marker

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“…They have a fairly high accuracy and reproducibility, but large time and economic costs also do not make them optimal for predicting food contamination. Mycological analysis, enzyme immunoassay, real-time PCR [1,2], and quantitative digital PCR, using markers based on intergenic spacers [3], are used to diagnose fusarium lesions. The common disadvantages of these methods are extremely expensive equipment and reagents, the duration of the analysis of up to 7-10 days, and the need for highly qualified specialists to conduct them.…”
Section: Introductionmentioning
confidence: 99%
“…They have a fairly high accuracy and reproducibility, but large time and economic costs also do not make them optimal for predicting food contamination. Mycological analysis, enzyme immunoassay, real-time PCR [1,2], and quantitative digital PCR, using markers based on intergenic spacers [3], are used to diagnose fusarium lesions. The common disadvantages of these methods are extremely expensive equipment and reagents, the duration of the analysis of up to 7-10 days, and the need for highly qualified specialists to conduct them.…”
Section: Introductionmentioning
confidence: 99%