• The detective method of ELISA which is convenient for clinical sample test was established.

    建立了ELISA诊断方法,为临床检测提供简便快捷的方法。

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  • Reintegration of a clinical or preclinical sample should be performed only under a predefined SOP.

    临床或临床前样品的再处理应仅根据预先确定的SOP进行。

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  • Users can build custom datasets by querying for specific clinical sample characteristics or copy number changes of individual genes.

    用户能够通过查询特定临床样品特征或个别基因的拷贝数变化构建定制的数据集。

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  • The sample scenario is based on the connected personal health model, which extends healthcare treatment beyond traditional clinical Settings into the patient's home.

    样例场景基于连接的个人健康模型,后者对医疗治理进行了扩展,超越了传统的临床模式,进入到患者的家里。

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  • Epidemiology investigation on AS: To adopt the multicenter, maximus sample clinical survey.

    AS临床流行病学调查:采用多中心,大样本临床调查。

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  • The study, published in The American Journal of Clinical Nutrition, has significant strengths in its prospective design, large sample and use of a well-validated dietary questionnaire.

    这项研究发表于《美国临床营养学杂志》(the AmericanJournalof Clinical Nutrition)。该研究因实验安排可操作、实验参与对象数量多并使用经充分验证过的饮食问卷调查而具有显著优势。

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  • Methods: 2060 cases of primary hepatic cancer were clinically researched by a large sample number clinical epidemiological survey program.

    方法:采用大样本临床流行病学调研方案,临床调查原发性肝癌2060例。

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  • The clinical date is analyed by t test and the ordinal date is analyed by two Independent Sample test.

    临床资料采用t检验,等级资料采用秩和检验进行统计分析。

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  • A randomly selected sample of 1003 of these participants were interiewed about personal and clinical parameters, including any history of malignancy.

    在这些参与者中随机选出1003 名做为样本,调查其个人和临床情况,其中包括所有恶性肿瘤史。

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  • Further multicenter randomized clinical trials of larger sample size are needed to compare the effects of SLED and CVVH on the outcomes of postsurgical acute dialysis patients.

    还需要进一步的多中心、随机、大样本临床实验来对比SLED和CVVH在术后紧急透析患者预后中的影响。

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  • Objective To study the sample size calculation of bioequivalence test in clinical trial.

    目的研究临床试验中等效性检验的样本量的计算问题。

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  • This result provides a theoretic basis for analysis of clinical emergency poisoning and sample collection of forensic poison analysis.

    本结果为氟安定临床急诊中毒分析和法医毒物分析的检材采取提供了理论依据。

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  • It works on the principle that aggregated data is currently only collected from a very small sample of cancer patients - the 4% which take part in registered clinical trials.

    它的工作原理是,目前只从癌症患者的一个非常小的样本收集数据,即有4%的患者参与注册临床试验。

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  • Methods: A sample of 157 pupils' emotion display rules and peer acceptance in third and fifth grades were tested by clinical interview and social nomination.

    方法:采用临床访谈和同伴提名法,考察157名三、五年级小学生的情绪表现规则和同伴接受性。

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  • A randomly selected sample of 1003 of these participants were interviewed about personal and clinical parameters, including any history of malignancy.

    在这些参与者中随机选出1003名做为样本,调查其个人和临床情况,其中包括所有恶性肿瘤史。

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  • Objective To establish a computer program for the management of sample and test item in clinical immunoassay.

    目的建立一种临床免疫学检验项目和标本的信息管理方法。

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  • Objective to establish a method to detect the antineutrophil antibodies in whole blood sample in clinical application in order to provide the evidences for the diagnosis of immune neutropenia.

    目的:建立可用于临床检测中性粒细胞抗体的方法,为诊断免疫性粒细胞减少症提供依据,并减少临床标本用血量。

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  • A single clinical tissue sample could generate many thousands of data points describing protein expression patterns.

    单个临床样本也会产生数以千计的描述蛋白表达模式的数据。

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  • Conclusion the procedure can be applied to determining the required sample sizes for the clinical trials with the purpose of discriminating the clinical significance of treatment control difference.

    结论对于以判别治疗-对照差临床意义为目的的临床试验,可用本文方法测定所需样本量。

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  • 6 secondary indicators, mainly contains personnel, equipment, sample collection, inspection reports, system and clinical feedback six indicators.

    6个二级指标,主要包含人员、设备、标本采集、检验报告、制度、临床反馈等6个方面指标。

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  • Methods Using barcode clinical laboratory information system, a module for management of sample and test item information was established.

    方法利用条形码检验信息管理系统,编制检验项目和标本管理模块。

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  • Methods Using barcode clinical laboratory information system, a module for management of sample and test item information was established.

    方法利用条形码检验信息管理系统,编制检验项目和标本管理模块。

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