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Respondent-driven sampling (RDS): The form of snowball sampling which starts with the recruitment of the small number of people in the target population to serve as the seeds. After participating the seeds are asked to recruit other people they know in target population. The sampling continues in this manner with the current sample members recruiting the next wave of the sample members until the desired sample size is achived. By using the mathematical model which weights the sample to compensate for the fact that the sample was collected in a non-random manner, the data provided by such a sampling scheme can be used to give asymptotically unbiased estimates about target population. An instance of the use of this approach is the estimation of the drug user's in New York who have HIV.
Consolidated Standards for Reporting Trials (CONSORT) statement : The protocol for reporting the results of the clinical trials. The core contribution of the statement comprises of
Computer-aided diagnosis : The computer programs which are designed to support clinical decision making. In common, such systems are based on the repeated application of the Bay
calculate absorbance value from concentration
Treatment allocation ratio is the ratio of the number of subjects allocated to the two treatments in a clinical trial. The equal allocation is most usual in practice, but it might
Relative risk is the measure of the association between the exposure to a particular factor and the risk or probability of a convinced outcome, calculated as follows therefor
The Null Hypothesis - H0: There is no heteroscedasticity i.e. β 1 = 0 The Alternative Hypothesis - H1: There is heteroscedasticity i.e. β 1 0 Reject H0 if Q = ESS/2 >
a shop is selling laptops at regular price and at half price.If the laptops are regular price a day they will be at regular price tha day after with proba 2/3, if the laptops are a
Missing Data - Reasons for screening data In case of any missing data, the researcher needs to conduct tests to ascertain that the pattern of these missing cases is random.
Protocol is the formal document outlining the proposed process for carrying out the clinical trial. The basic features of the document are to study the objectives, patient selecti
Ordination is the procedure of reducing the dimensionality (that is the number of variables) of multivariate data by deriving the small number of new variables which contain much
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