This document provides an overview of receiver operating characteristic (ROC) curves. It defines an ROC curve as a graphical plot that illustrates the performance of a binary classifier system by varying its discrimination threshold. An ROC curve plots the true positive rate against the false positive rate. The area under the ROC curve (AUC) provides a single measure of classifier performance, where an AUC of 1 represents a perfect classifier and 0.5 represents a random classifier. The document discusses how ROC curves can be used to compare multiple classifiers and select optimal threshold values to balance sensitivity and specificity.
How to read a receiver operating characteritic (ROC) curveSamir Haffar
1) The document discusses how to evaluate the accuracy of diagnostic tests using receiver operating characteristic (ROC) curves.
2) ROC curves plot the sensitivity of a test on the y-axis against 1-specificity on the x-axis. The area under the ROC curve (AUC) provides an overall measure of a test's accuracy, with higher values indicating better accuracy.
3) The document uses ferritin testing to diagnose iron deficiency anemia (IDA) in the elderly as a case example. The AUC for ferritin was found to be 0.91, indicating it is an excellent test for diagnosing IDA.
Sample size calculation for cohort studies Subhashini N
This document discusses sample size calculations for different types of cohort studies. It provides examples of calculating sample sizes for studies measuring one variable, differences between two means, rates, or proportions. The key factors considered are the confidence interval, power, estimated outcomes in exposed and unexposed groups, and standard deviation or error terms. Sample size formulas are provided for prospective and retrospective cohort studies comparing outcomes within or between groups.
Sample size calculations are an important step in planning epidemiological studies. An adequate sample size is needed to ensure reliable results, while samples that are too large or small can lead to wasted resources or inaccurate findings. Different study designs require different sample size calculation methods. Factors considered include the desired precision or confidence level, population parameters, and variability. Several formulas and online calculators exist to determine appropriate sample sizes for estimating means, proportions, and comparing groups in studies like clinical trials, surveys, case-control studies, and experiments. Larger effects, more samples, less variability, and higher significance levels can increase a test's statistical power.
Sensitivity, specificity and likelihood ratiosChew Keng Sheng
A short tutorial on sensitivity, specificity and likelihood ratios. In this presentation, I demonstrate why likelihood ratios are better parameters compared to sensitivity and specificity in real world setting.
Confidence Intervals: Basic concepts and overviewRizwan S A
This document provides an overview of confidence intervals. It defines confidence intervals and describes their use in statistical inference to estimate population parameters. It explains that a confidence interval provides a range of plausible values for an unknown population parameter based on a sample statistic. The document outlines the key steps in calculating a confidence interval, including determining the point estimate, standard error, and critical value corresponding to the desired confidence level. It discusses how the width of the confidence interval indicates the precision of the estimate and is affected by factors like the sample size and population variability.
This document provides an overview of biostatistics concepts. It defines biostatistics as the application of statistics to biological and medical topics. Biostatisticians play roles in designing studies, analyzing data, and interpreting results. They apply statistical methods to address questions in public health, medicine, and environmental biology. The document outlines different types of variables, such as categorical, ordinal, interval and ratio variables. It also distinguishes between populations and samples, and between random and non-random sampling. Finally, it discusses different levels of measurement and categories of data in biostatistics.
This document provides an overview of chi square tests as a type of non-parametric statistic. It explains that chi square tests are used to analyze nominal or categorical data by comparing observed frequencies to expected frequencies if the null hypothesis is true. An example is provided to demonstrate how to calculate chi square values from a contingency table and determine significance based on degrees of freedom and p-values. The document also outlines other types of non-parametric tests that can be used depending on whether the data is nominal, ordinal, independent, or matched samples.
This document discusses predictive value, likelihood ratios, and how to calculate and apply them. Predictive value reflects a test's diagnostic power and depends on sensitivity, specificity, and disease prevalence. The positive predictive value is the probability a positive test truly has the disease, while the negative predictive value is the probability a negative test truly doesn't have the disease. Likelihood ratios compare true positives and negatives to false ones to determine if a test result changes the probability a disease is present.
This document defines odds ratio and describes how to calculate and interpret it. An odds ratio measures the association between two events and compares the odds of one event occurring given the presence or absence of the other event. The document provides an example to calculate the odds ratio to determine if having a mutated gene increases the odds of cancer. It also defines confidence intervals and how they provide a range of values that likely contain the true population parameter based on a sample. Confidence intervals allow flexible data analysis and meaningful conclusions, especially for small sample studies.
This document discusses sample size calculation for a cohort study. It provides an example comparing the risk of diabetes mellitus (DM) between overweight and normal weight adults. Based on prior literature showing DM rates of 32% in overweight adults and 7% in normal weight adults, the required sample size is calculated as 38 subjects for each group, for a total of 76 subjects. The document also discusses using online calculators or formulas to manually calculate sample sizes and considers approaches if there is no prior information available.
A sample design is a definite plan for obtaining a sample from a given population. Researcher must select/prepare a sample design which should be reliable and appropriate for his research study.
Introduction to statistics and graphical representationAMNA BUTT
This document provides an introduction to statistics, including definitions and types. It discusses descriptive statistics, which deals with summarizing and describing numerical data through tables, graphs, and measures of center. Inferential statistics makes inferences about populations based on samples. The document also covers graphical representations in statistics, such as bar graphs, line graphs, pie charts, pictograms, and histograms, which visually display statistical data.
The document discusses odds ratios, which are used to measure the association between an exposure and an outcome. An odds ratio is calculated by dividing the odds of an event in one group (e.g. exposed to a drug) by the odds of the event in another unexposed group. Odds ratios can be calculated in both cohort and case-control studies. While relative risk can only be calculated in cohort studies, odds ratios are commonly used to approximate relative risk in case-control studies when the outcome is rare. The document provides examples of how to calculate odds ratios from 2x2 contingency tables and interprets what different values mean.
This document discusses sample size determination and calculation. It defines sample size as the subset of a population chosen for a study to make inferences about the total population. The key factors in determining sample size are the desired level of accuracy, allowing for appropriate analysis, and validity of significance tests. The document provides formulas and methods for calculating sample size for different study designs and populations, including using formulas, readymade tables, nomograms, and computer software. Accurately determining sample size is essential for research.
In clinical trials and other scientific studies, an interim analysis is an analysis of data that is conducted before data collection has been completed. If a treatment is particularly beneficial or harmful compared to the concurrent placebo group while the study is on-going, the investigators are ethically obliged to assess that difference using the data at hand and to make a deliberate consideration of terminating the study earlier than planned.
In interim analysis, whenever a new drug shows adverse effect on human being while testing the effectiveness of several drugs, we immediately stop the trial by taking into account the fact that maximum number of patients receive most effective treatment at the earliest stage. Interim analysis is also used to possibly reduce the expected number of patients and to shorten the follow-up time needed to make a conclusion. One wouldn't have to spend extra money if he/she already have enough evidence about the outcome. In this presentation, the total sample size is divided into four equal parts to perform the analysis and decision is made based on each individual step.
This document discusses various statistical tests used to analyze categorical data, including contingency tables and chi-square tests. It begins by defining continuous and categorical variables. It then discusses how to represent associations between categorical variables using contingency tables. It explains how to calculate expected frequencies and chi-square values to test for relationships between categorical variables. Finally, it discusses other tests that can be used for contingency tables like Fisher's exact test, McNemar's test, and Yates correction.
This document discusses key statistical concepts including p-values, type I and II errors, power, and sample size. It defines p-value as the probability of obtaining results as extreme or more extreme than what was observed. Type I error is rejecting the null hypothesis when it is true, while type II error is failing to reject the null when it is false. Power is the probability of avoiding a type II error. The relationships between these concepts and how factors like sample size and effect size influence them are explained. Sample size calculations must consider the desired power, significance level, population variability, and minimum effect size to detect.
This document discusses various statistical tests used to analyze agreement between raters or tests, including intraclass correlation, Cohen's kappa, and Bland-Altman plots. It explains how to perform intraclass correlation, Cohen's kappa, receiver operating characteristic curves, and other tests on SPSS. These statistical analyses are used to evaluate rater agreement, compare tests to a gold standard, and determine if tests provide predictions better than chance. The document provides guidance on interpreting the results of these analyses and choosing appropriate cut-off values.
4. Calculate samplesize for cross-sectional studiesAzmi Mohd Tamil
This document discusses sample size calculations for a comparative cross-sectional study to prove an association between a risk factor and outcome. It provides an example calculating the sample size needed to show Indians have a higher risk of diabetes compared to other races in Malaysia. The calculations are shown manually and using online calculators StatCalc and PS2. While the manual and StatCalc methods agree, PS2 produces a different result. Prior literature on disease rates and the risk factor is needed for sample size calculations.
Variables describe attributes that can vary between entities. They can be qualitative (categorical) or quantitative (numeric). Common types of variables include continuous, discrete, ordinal, and nominal variables. Data can be presented graphically through bar charts, pie charts, histograms, box plots, and scatter plots to better understand patterns and trends. Key measures used to summarize data include measures of central tendency (mean, median, mode) and measures of variability (range, standard deviation, interquartile range).
Lecture of Respected Sir Dr. L.M. BEHERA from N.I.H. KOLKATA in a workshop at G.D.M.H.M.C. - Patna in the Year 2011.
SUBJECT : BIOSTATISTICS
TOPIC : 'INTRODUCTION TO BIOSTATISTICS'.
Superiority, Equivalence, and Non-Inferiority Trial DesignsKevin Clauson
http://bit.ly/bQKcGz This lecture was presented as part of the Drug Literature Evaluation course at Nova Southeastern University. Guided notes and an audience response system were used to augment to lecture. Context for my decision to share these slides can be found at the provided link.
Box plots provide a standardized way to display data distribution based on number summaries. They show outliers and values, whether data is symmetrical or skewed, and how tightly grouped data is. A box plot constructs from minimum, first quartile, median, third quartile, and maximum values. It divides data into sections containing approximately 25% of values each. Box plots summarize data in a way that allows researchers to quickly identify mean values, dispersion, and signs of skewness. Grouped box plots are used to compare multiple groups on the same quantitative outcomes.
When you perform a hypothesis test in statistics, a p-value helps you determine the significance of your results. ... The p-value is a number between 0 and 1 and interpreted in the following way: A small p-value (typically ≤ 0.05) indicates strong evidence against the null hypothesis, so you reject the null hypothesis.
This document defines data and different types of data presentation. It discusses quantitative and qualitative data, and different scales for qualitative data. The document also covers different ways to present data scientifically, including through tables, graphs, charts and diagrams. Key types of visual presentation covered are bar charts, histograms, pie charts and line diagrams. Presentation should aim to clearly convey information in a concise and systematic manner.
This document discusses sample size calculation and determination. It begins by defining a sample as a subset of a population used to make inferences about the whole population. Several factors affect sample size, including required accuracy, available resources, and desired level of precision. The document outlines different formulas and methods for calculating sample size based on study design and outcome measures. It provides examples of calculating sample size for estimating means, proportions, rates, odds ratios, and risk ratios. Computer software and readymade tables can also be used to determine optimal sample sizes.
This document provides an overview of survival analysis. It defines key terms like survival, censoring, and hazard functions. It describes the Kaplan-Meier method for estimating survival functions from censored data and comparing survival curves between groups using the log-rank test. Censoring occurs when subjects are lost to follow-up before the event of interest. The Kaplan-Meier method accounts for censoring to calculate the probability of surviving up to different time points.
The document discusses various statistical concepts related to hypothesis testing, including:
- Types I and II errors that can occur when testing hypotheses
- How the probability of committing errors depends on factors like the sample size and how far the population parameter is from the hypothesized value
- The concept of critical regions and how they are used to determine if a null hypothesis can be rejected
- The difference between discrete and continuous probability distributions and examples of each
- How an observed test statistic is calculated and compared to a critical value to determine whether to reject or not reject the null hypothesis
Testing differences between means_The Basicskbernhardt2013
This document discusses different tests for comparing means, including t-tests and ANOVAs. It provides guidance on when to use a t-test versus z-test based on sample size. Key points covered include defining the null and alternative hypotheses, setting the alpha level to determine statistical significance, and interpreting the standard error of the mean when comparing sample means to population means. Graphs and equations are presented for finding critical values and calculating the probability of obtaining a given sample mean.
This document discusses predictive value, likelihood ratios, and how to calculate and apply them. Predictive value reflects a test's diagnostic power and depends on sensitivity, specificity, and disease prevalence. The positive predictive value is the probability a positive test truly has the disease, while the negative predictive value is the probability a negative test truly doesn't have the disease. Likelihood ratios compare true positives and negatives to false ones to determine if a test result changes the probability a disease is present.
This document defines odds ratio and describes how to calculate and interpret it. An odds ratio measures the association between two events and compares the odds of one event occurring given the presence or absence of the other event. The document provides an example to calculate the odds ratio to determine if having a mutated gene increases the odds of cancer. It also defines confidence intervals and how they provide a range of values that likely contain the true population parameter based on a sample. Confidence intervals allow flexible data analysis and meaningful conclusions, especially for small sample studies.
This document discusses sample size calculation for a cohort study. It provides an example comparing the risk of diabetes mellitus (DM) between overweight and normal weight adults. Based on prior literature showing DM rates of 32% in overweight adults and 7% in normal weight adults, the required sample size is calculated as 38 subjects for each group, for a total of 76 subjects. The document also discusses using online calculators or formulas to manually calculate sample sizes and considers approaches if there is no prior information available.
A sample design is a definite plan for obtaining a sample from a given population. Researcher must select/prepare a sample design which should be reliable and appropriate for his research study.
Introduction to statistics and graphical representationAMNA BUTT
This document provides an introduction to statistics, including definitions and types. It discusses descriptive statistics, which deals with summarizing and describing numerical data through tables, graphs, and measures of center. Inferential statistics makes inferences about populations based on samples. The document also covers graphical representations in statistics, such as bar graphs, line graphs, pie charts, pictograms, and histograms, which visually display statistical data.
The document discusses odds ratios, which are used to measure the association between an exposure and an outcome. An odds ratio is calculated by dividing the odds of an event in one group (e.g. exposed to a drug) by the odds of the event in another unexposed group. Odds ratios can be calculated in both cohort and case-control studies. While relative risk can only be calculated in cohort studies, odds ratios are commonly used to approximate relative risk in case-control studies when the outcome is rare. The document provides examples of how to calculate odds ratios from 2x2 contingency tables and interprets what different values mean.
This document discusses sample size determination and calculation. It defines sample size as the subset of a population chosen for a study to make inferences about the total population. The key factors in determining sample size are the desired level of accuracy, allowing for appropriate analysis, and validity of significance tests. The document provides formulas and methods for calculating sample size for different study designs and populations, including using formulas, readymade tables, nomograms, and computer software. Accurately determining sample size is essential for research.
In clinical trials and other scientific studies, an interim analysis is an analysis of data that is conducted before data collection has been completed. If a treatment is particularly beneficial or harmful compared to the concurrent placebo group while the study is on-going, the investigators are ethically obliged to assess that difference using the data at hand and to make a deliberate consideration of terminating the study earlier than planned.
In interim analysis, whenever a new drug shows adverse effect on human being while testing the effectiveness of several drugs, we immediately stop the trial by taking into account the fact that maximum number of patients receive most effective treatment at the earliest stage. Interim analysis is also used to possibly reduce the expected number of patients and to shorten the follow-up time needed to make a conclusion. One wouldn't have to spend extra money if he/she already have enough evidence about the outcome. In this presentation, the total sample size is divided into four equal parts to perform the analysis and decision is made based on each individual step.
This document discusses various statistical tests used to analyze categorical data, including contingency tables and chi-square tests. It begins by defining continuous and categorical variables. It then discusses how to represent associations between categorical variables using contingency tables. It explains how to calculate expected frequencies and chi-square values to test for relationships between categorical variables. Finally, it discusses other tests that can be used for contingency tables like Fisher's exact test, McNemar's test, and Yates correction.
This document discusses key statistical concepts including p-values, type I and II errors, power, and sample size. It defines p-value as the probability of obtaining results as extreme or more extreme than what was observed. Type I error is rejecting the null hypothesis when it is true, while type II error is failing to reject the null when it is false. Power is the probability of avoiding a type II error. The relationships between these concepts and how factors like sample size and effect size influence them are explained. Sample size calculations must consider the desired power, significance level, population variability, and minimum effect size to detect.
This document discusses various statistical tests used to analyze agreement between raters or tests, including intraclass correlation, Cohen's kappa, and Bland-Altman plots. It explains how to perform intraclass correlation, Cohen's kappa, receiver operating characteristic curves, and other tests on SPSS. These statistical analyses are used to evaluate rater agreement, compare tests to a gold standard, and determine if tests provide predictions better than chance. The document provides guidance on interpreting the results of these analyses and choosing appropriate cut-off values.
4. Calculate samplesize for cross-sectional studiesAzmi Mohd Tamil
This document discusses sample size calculations for a comparative cross-sectional study to prove an association between a risk factor and outcome. It provides an example calculating the sample size needed to show Indians have a higher risk of diabetes compared to other races in Malaysia. The calculations are shown manually and using online calculators StatCalc and PS2. While the manual and StatCalc methods agree, PS2 produces a different result. Prior literature on disease rates and the risk factor is needed for sample size calculations.
Variables describe attributes that can vary between entities. They can be qualitative (categorical) or quantitative (numeric). Common types of variables include continuous, discrete, ordinal, and nominal variables. Data can be presented graphically through bar charts, pie charts, histograms, box plots, and scatter plots to better understand patterns and trends. Key measures used to summarize data include measures of central tendency (mean, median, mode) and measures of variability (range, standard deviation, interquartile range).
Lecture of Respected Sir Dr. L.M. BEHERA from N.I.H. KOLKATA in a workshop at G.D.M.H.M.C. - Patna in the Year 2011.
SUBJECT : BIOSTATISTICS
TOPIC : 'INTRODUCTION TO BIOSTATISTICS'.
Superiority, Equivalence, and Non-Inferiority Trial DesignsKevin Clauson
http://bit.ly/bQKcGz This lecture was presented as part of the Drug Literature Evaluation course at Nova Southeastern University. Guided notes and an audience response system were used to augment to lecture. Context for my decision to share these slides can be found at the provided link.
Box plots provide a standardized way to display data distribution based on number summaries. They show outliers and values, whether data is symmetrical or skewed, and how tightly grouped data is. A box plot constructs from minimum, first quartile, median, third quartile, and maximum values. It divides data into sections containing approximately 25% of values each. Box plots summarize data in a way that allows researchers to quickly identify mean values, dispersion, and signs of skewness. Grouped box plots are used to compare multiple groups on the same quantitative outcomes.
When you perform a hypothesis test in statistics, a p-value helps you determine the significance of your results. ... The p-value is a number between 0 and 1 and interpreted in the following way: A small p-value (typically ≤ 0.05) indicates strong evidence against the null hypothesis, so you reject the null hypothesis.
This document defines data and different types of data presentation. It discusses quantitative and qualitative data, and different scales for qualitative data. The document also covers different ways to present data scientifically, including through tables, graphs, charts and diagrams. Key types of visual presentation covered are bar charts, histograms, pie charts and line diagrams. Presentation should aim to clearly convey information in a concise and systematic manner.
This document discusses sample size calculation and determination. It begins by defining a sample as a subset of a population used to make inferences about the whole population. Several factors affect sample size, including required accuracy, available resources, and desired level of precision. The document outlines different formulas and methods for calculating sample size based on study design and outcome measures. It provides examples of calculating sample size for estimating means, proportions, rates, odds ratios, and risk ratios. Computer software and readymade tables can also be used to determine optimal sample sizes.
This document provides an overview of survival analysis. It defines key terms like survival, censoring, and hazard functions. It describes the Kaplan-Meier method for estimating survival functions from censored data and comparing survival curves between groups using the log-rank test. Censoring occurs when subjects are lost to follow-up before the event of interest. The Kaplan-Meier method accounts for censoring to calculate the probability of surviving up to different time points.
The document discusses various statistical concepts related to hypothesis testing, including:
- Types I and II errors that can occur when testing hypotheses
- How the probability of committing errors depends on factors like the sample size and how far the population parameter is from the hypothesized value
- The concept of critical regions and how they are used to determine if a null hypothesis can be rejected
- The difference between discrete and continuous probability distributions and examples of each
- How an observed test statistic is calculated and compared to a critical value to determine whether to reject or not reject the null hypothesis
Testing differences between means_The Basicskbernhardt2013
This document discusses different tests for comparing means, including t-tests and ANOVAs. It provides guidance on when to use a t-test versus z-test based on sample size. Key points covered include defining the null and alternative hypotheses, setting the alpha level to determine statistical significance, and interpreting the standard error of the mean when comparing sample means to population means. Graphs and equations are presented for finding critical values and calculating the probability of obtaining a given sample mean.
This document discusses hypothesis testing and significance tests. It defines key terms like parameters, statistics, sampling distribution, standard error, null and alternative hypotheses, type I and type II errors. It explains how to set up a hypothesis test, including choosing a significance level and critical value. Both one-tailed and two-tailed tests are described. Finally, it provides an overview of different types of significance tests for both large and small sample sizes.
C2 st lecture 10 basic statistics and the z test handoutfatima d
This document provides an overview of basic statistics concepts including averages, measures of dispersion, hypothesis testing, and the z-test. It defines the mode, median, mean, interquartile range, standard deviation, and absolute deviation. It explains how to perform a z-test including writing the null and alternative hypotheses, looking up the critical value, calculating the test statistic, and making a decision. Two examples of z-tests are provided to demonstrate the process.
1) The document discusses hypothesis testing and statistical inference using examples related to coin tossing. It explains the concepts of type I and type II errors and how hypothesis tests are conducted.
2) An example is provided to test the hypothesis that the average American ideology is somewhat conservative (H0: μ = 5) using data from the National Election Study. The alternative hypothesis is that the average is less than 5 (HA: μ < 5).
3) The results of the hypothesis test show the observed test statistic is lower than the critical value, so the null hypothesis that the average is 5 is rejected in favor of the alternative that the average is less than 5.
- The document discusses hypothesis testing using regression analysis, focusing on the confidence interval approach and test of significance approach.
- It provides an example using wage and education data to test the hypothesis that the slope coefficient is equal to 0.5. Both the confidence interval approach and t-test approach are used to reject the null hypothesis.
- One-tailed and two-tailed hypothesis tests are explained. Additional topics covered include choosing the significance level, statistical versus practical significance, and reporting the results of regression analysis.
WEEK 6 – HOMEWORK 6 LANE CHAPTERS, 11, 12, AND 13; ILLOWSKY CHAP.docxcockekeshia
WEEK 6 – HOMEWORK 6: LANE CHAPTERS, 11, 12, AND 13; ILLOWSKY CHAPTERS 9, 10
INTRODUCTION TO HYPOTHESIS TESTING
WHAT IS A HYPOTHESIS TEST?
Here we are testing claims about the TRUE POPULATION’S STATISTICS based on SAMPLES we have taken. The most common statistic of interest is of course the POPULATION MEAN (µ). But, we can also test its VARIANCE and its STANDARD DEVIATION. (We can also compare TWO or more means to see if there are significant differences.
We must have a basic hypothesis, referred to as the NULL Hypothesis (Ho) and an ALTERNATE Hypothesis (Ha).
Our NULL ( and ALTERNATE) Hypotheses can take three forms:
(1) Ho: µ< some number; Ha: µ > that number (< is “less than or equal to” and > is “greater than or equal to” ),
(2) Ho: µ> some number; Ha: µ < that number , or
(3) Ho: µ = some number; Ha µ≠ that number ; (≠ means “not equal to”)
NOTE THAT Ho MUST HAVE THE “EQUALS” IN IT WHEREAS Ha NEVER DOES.
(1) Is referred to as a “ONE-TAILED TEST TO THE LEFT”
(2) Is a “ONE-TAILED TEST TO THE RIGHT”
(3) Is a “TWO-TAILED TEST”
NEXT, we need to decide what level of significance, i.e.(how sure we want to be about our hypothesis. This is where α comes in again. Do we want to test at the 10%, 5% or 1% level of significance? Another wrinkle is that for the TWO-TAILED test, since our value could be greater OR less than some number, we use α /2 for each extreme, so for 10% it’s 5% (0.050) at each end (tail of the curve), for 5% it’s 2.5% (0.0250) at each end, and for 1% it’s 0.5% (0.0050) at the ends. You have heard about this kind of split before with confidence intervals, but think about it. Here is a graphical display of all this:
As you can see, there is a CRITICAL z-VALUE for each of these test depending on the significance level alpha (α) or α/2.
In HW4 questions 1 and 2, you found the critical z-values for alpha’s of 1%, 5% and 10%, which would work for the one-tailed tests. For the two tailed tests we need to split these alphas (α/2) and find the critical z-values (at the positive and negative tails of the graph) So, for an α of 1% (0.0100) it would be α/2 or 0.005 in the left tail (negative z-value) = -2.575 and for the far right tail (0.005 in that tail) we would have to find the z-value for an area to the LEFT of 99.5% (0.9950) and this is +z = +2.575
Continuing on, for an α of 5% for a two-tailed test the z-values for α/2 would correspond to areas under the curve of 0.0250 at each end. The far left tail would have a negative z-value of -1.96 (see picture above) and the far right tail would have a positive z-value of +1.96 that in the Table represented an area of 97.5% (0.9750) to the LEFT.
Lastly, for an alpha of 10%, hence an α/2 at both ends of 5% (the two-tailed test), the negative z-value would be -1.645.
The positive z-value marking the upper 5% (Table value from 95% to the left) is +1.645.
SO, FOR YOUR USE IN ALL HYPOTHESIS TEST (AND WORKS FOR CONFIDENCE INTERVALS TOO) .
PAGE
O&M Statistics – Inferential Statistics: Hypothesis Testing
Inferential Statistics
Hypothesis testing
Introduction
In this week, we transition from confidence intervals and interval estimates to hypothesis testing, the basis for inferential statistics. Inferential statistics means using a sample to draw a conclusion about an entire population. A test of hypothesis is a procedure to determine whether sample data provide sufficient evidence to support a position about a population. This position or claim is called the alternative or research hypothesis.
“It is a procedure based on sample evidence and probability theory to determine whether the hypothesis is a reasonable statement” (Mason & Lind, pg. 336).
This Week in Relation to the Course
Hypothesis testing is at the heart of research. In this week, we examine and practice a procedure to perform tests of hypotheses comparing a sample mean to a population mean and a test of hypotheses comparing two sample means.
The Five-Step Procedure for Hypothesis Testing (you need to show all 5 steps – these contain the same information you would find in a research paper – allows others to see how you arrived at your conclusion and provides a basis for subsequent research).
Step 1
State the null hypothesis – equating the population parameter to a specification. The null hypothesis is always one of status quo or no difference. We call the null hypothesis H0 (H sub zero). It is the hypothesis that contains an equality.
State the alternate hypothesis – The alternate is represented as H1 or HA (H sub one or H sub A). The alternate hypothesis is the exact opposite of the null hypothesis and represents the conclusion supported if the null is rejected. The alternate will not contain an equal sign of the population parameter.
Most of the time, researchers construct tests of hypothesis with the anticipation that the null hypothesis will be rejected.
Step 2
Select a level of significance (α) which will be used when finding critical value(s).
The level you choose (alpha) indicates how confident we wish to be when making the decision.
For example, a .05 alpha level means that we are 95% sure of the reliability of our findings, but there is still a 5% chance of being wrong (what is called the likelihood of committing a Type 1 error).
The level of significance is set by the individual performing the test. Common significance levels are .01, .05, and .10. It is important to always state what the chosen level of significance is.
Step 3
Identify the test statistic – this is the formula you use given the data in the scenario. Simply put, the test statistic may be a Z statistic, a t statistic, or some other distribution. Selection of the correct test statistic will depend on the nature of the data being tested (sample size, whether the population standard deviation is known, whether the data is known to be normally distributed).
The sampling distribution of the test statistic is divided into t.
Bio-statistics definitions and misconceptionsQussai Abbas
The document discusses null and alternative hypotheses when looking at two or more groups that differ based on a treatment or risk factor. The null hypothesis assumes there is no difference between groups, while the alternative hypothesis assumes a difference. By default, the null hypothesis is assumed to be true until evidence supports rejecting it in favor of the alternative. Type I and type II errors in hypothesis testing are explained, along with the level of significance, p-values, and how confidence intervals can be used to determine if results are statistically significant. Methods for visualizing relationships between variables like scatter plots, calculating Pearson's correlation coefficient, and using regression analysis are also summarized.
Steps of hypothesis testingSelect the appropriate testSo far.docxdessiechisomjj4
Steps of hypothesis testing
Select the appropriate test
So far we’ve learned a couple variation on z- and t-tests
See next slide for how to select
State your research hypothesis and your null hypothesis
State them in English
Then in math
Describe the NULL distribution
Starting here is where you be a skeptic and assume the null is true!
For one-sample tests, you will need to determine μ
(For two-tailed tests, you don’t need to worry about μ)
Compute the relevant standard error
Determine your critical value(s)
Keep in mind whether it is a directional or non-directional test
Compute the test statistic
Compare the test stat to the critical value(s) and make your decision
When to use each test
All of these tests require that the sampling distribution is normal
Either because population is normal or, thanks to central limit theorem, sample size is very large
All of these tests require that the measures be quantitative variables, that is interval/ratio
(Not all quantitative variables are normal, BUT all normal variables are quantitative. So if someone tells you a variable is normal, you know it is also quantitative.)
When to use each test, cont’d
1 Sample z-test
Comparing one sample mean to a population mean
And you do know σ (population SD)
2 sample z-test
Comparing two sample means to each other
And you do know σM1-M2 (standard error of difference of means)
1 sample t-test
Comparing one sample mean to a population mean
You only know s (sample SD)
2 sample t-test
Comparing two sample means to each other
You only know s1 and s2 (sample SDs)
Dependent sample t-test
You have two scores coming from each person, such as if you measured them before and after an experimental manipulation.
Compute the differences between the two scores, then treat like a 1 sample t
What is α?
Put on your skeptic’s hat: you believe the null hypothesis is true
But you’re willing to be convinced you’re wrong
If the test statistic is sufficiently improbable, you will change your mind and decide the null hypothesis is false
What is “sufficiently” improbable?
When your test statistic is more extreme than your critical values
Critical values are selected so that only a small fraction of the entire distribution is more extreme than the critical values
This “small fraction” is called α
Conventionally, α is usually set to .05, that is 5%
Directionality of a test
Is a test simply about whether there a difference, regardless of direction?
If so, it is a non-directed, or undirected, or two-tailed test
Your α must be evenly split between the two tails
For the conventional α = .05, that means each tail should have .025 or 2.5% of the total distribution
Is the test predicting one mean will be bigger than another? Or is it predicting one mean will be less than another?
If so, it a directional, or directed, or one-tailed test
Put all your α in a single tail
Special note on one-tailed tests
Step 3 of our procedure is a little awkward when we have one-tailed tests
How do you descr.
A prospective study is designed to compare the sensitivity and specificity of a new diagnostic test to an existing test using binomial tests. The power of the study is determined for sensitivity increases of 10-25% and a specificity increase of 10%, sample sizes of 300 to 3000, a prevalence of 6%, and a significance level of 5%. With a sample size of 300, the power is 8.7% for detecting a 10% sensitivity increase and 97.2% for detecting the 10% specificity increase. Larger sample sizes result in higher power to detect the sensitivity increases.
ders 3.2 Unit root testing section 2 .pptxErgin Akalpler
The document provides information about several theoretical probability distributions including the normal, t, and chi-square distributions. It discusses their key properties and formulas. For the normal distribution, it covers the empirical rule, skewness, kurtosis, and how to calculate z-scores. Examples are given for finding areas under the normal curve and performing hypothesis tests using the t and chi-square distributions.
The document provides information about several theoretical probability distributions including the normal, t, and chi-square distributions. It discusses key properties such as the mean, standard deviation, and shape of the normal distribution curve. Examples are given to demonstrate how to calculate areas under the normal distribution curve and find z-scores. The t-distribution is introduced as similar to the normal but used for smaller sample sizes. The chi-square distribution is defined as used for hypothesis testing involving categorical data.
Application of Statistical and mathematical equations in Chemistry Part 2Awad Albalwi
Application of Statistical and mathematical equations in Chemistry
Part 2
Accuracy
Precision
Propagation of Error
Confidence Limits
F-Test Values
Student’s t-test
Paired Sample t-test
Q test
Least Squares Method
correlation coefficient
This document provides an overview of probability theory, including key definitions, concepts, and calculations. It discusses:
1. Definitions of probability, including the frequency and subjective concepts. It also defines basic terminology like experiments, trials, outcomes, and events.
2. Methods of calculating probability, including classical and empirical approaches. It presents the classical probability formula.
3. Common probability distributions like the binomial distribution and normal distribution. It provides examples of calculating probabilities using these distributions.
4. Additional probability concepts like independent and conditional probability, random variables, and transformations to the standardized normal distribution.
5. The importance of the normal distribution in applications like medicine, sampling, and statistical significance testing. It
The document discusses key concepts in statistical inference including estimation, confidence intervals, hypothesis testing, and types of errors. It provides examples and formulas for estimating population means from sample data, calculating confidence intervals, stating the null and alternative hypotheses, and making decisions to accept or reject the null hypothesis based on a significance level.
This document provides an overview of key concepts in hypothesis testing including:
- The null and alternative hypotheses, where the null hypothesis is what we aim to reject or fail to reject.
- The level of significance and critical region, which define the threshold for rejecting the null hypothesis.
- Type I and type II errors, where we aim to minimize both by choosing an appropriate significance level and critical region.
- Common test statistics like z, t, and chi-squared that are used to evaluate hypotheses based on samples.
- The process of hypothesis testing, which involves defining hypotheses, choosing a test statistic and significance level, and making a decision to reject or fail to reject the null based on the critical region.
Answer the questions in one paragraph 4-5 sentences. · Why did t.docxboyfieldhouse
Answer the questions in one paragraph 4-5 sentences.
· Why did the class collectively sign a blank check? Was this a wise decision; why or why not? we took a decision all the class without hesitation
· What is something that I said individuals should always do; what is it; why wasn't it done this time? Which mitigation strategies were used; what other strategies could have been used/considered? individuals should always participate in one group and take one decision
SAMPLING MEAN:
DEFINITION:
The term sampling mean is a statistical term used to describe the properties of statistical distributions. In statistical terms, the sample meanfrom a group of observations is an estimate of the population mean. Given a sample of size n, consider n independent random variables X1, X2... Xn, each corresponding to one randomly selected observation. Each of these variables has the distribution of the population, with mean and standard deviation. The sample mean is defined to be
WHAT IT IS USED FOR:
It is also used to measure central tendency of the numbers in a database. It can also be said that it is nothing more than a balance point between the number and the low numbers.
HOW TO CALCULATE IT:
To calculate this, just add up all the numbers, then divide by how many numbers there are.
Example: what is the mean of 2, 7, and 9?
Add the numbers: 2 + 7 + 9 = 18
Divide by how many numbers (i.e., we added 3 numbers): 18 ÷ 3 = 6
So the Mean is 6
SAMPLE VARIANCE:
DEFINITION:
The sample variance, s2, is used to calculate how varied a sample is. A sample is a select number of items taken from a population. For example, if you are measuring American people’s weights, it wouldn’t be feasible (from either a time or a monetary standpoint) for you to measure the weights of every person in the population. The solution is to take a sample of the population, say 1000 people, and use that sample size to estimate the actual weights of the whole population.
WHAT IT IS USED FOR:
The sample variance helps you to figure out the spread out in the data you have collected or are going to analyze. In statistical terminology, it can be defined as the average of the squared differences from the mean.
HOW TO CALCULATE IT:
Given below are steps of how a sample variance is calculated:
· Determine the mean
· Then for each number: subtract the Mean and square the result
· Then work out the mean of those squared differences.
To work out the mean, add up all the values then divide by the number of data points.
First add up all the values from the previous step.
But how do we say "add them all up" in mathematics? We use the Roman letter Sigma: Σ
The handy Sigma Notation says to sum up as many terms as we want.
· Next we need to divide by the number of data points, which is simply done by multiplying by "1/N":
Statistically it can be stated by the following:
·
· This value is the variance
EXAMPLE:
Sam has 20 Rose Bushes.
The number of flowers on each b.
This document discusses inferential statistics and epidemiological research. It introduces concepts like the central limit theorem, standard error, confidence intervals, hypothesis testing, and different statistical tests. Specifically, it covers:
- The central limit theorem states that sample means will follow a normal distribution, even if the population is not normally distributed.
- Standard error is used to measure sampling variation and determine confidence intervals around sample statistics to estimate population parameters.
- Hypothesis testing involves a null hypothesis of no difference and an alternative hypothesis of a significant difference.
- Common tests discussed include chi-square tests to compare proportions between groups and determine if differences are significant.
Essential Drugs Dosage and Formulations (Medical Booklet Series by Dr. Aryan ...Dr. Aryan (Anish Dhakal)
This is the 22nd part of medical booklet series created by Dr. Aryan in order to familiarize doctors and medical students about the basic doses of drugs. Many students remember the mechanism of actions and other details of drug very well and regard doses as unnecessary. While you prescribe, this becomes one of the most important aspect. This study material is focused to resolve such issues.
Osteoarthritis is a chronic degenerative disorder of synovial joints in which there is progressive softening and erosion/disintegration of the articular cartilage. In the presentation, I will deal in detail about the condition in every dimension with the most recent evidence.
Preterm labor is the labor that starts before the 37th completed week. In this presentation, we will discover causes, pathogenesis, diagnosis, clinical features, and management principles for preterm labor along with the most recent evidence.
Delirium, also referred to as "acute confusional state" or "acute brain syndrome," is a condition of severe confusion and rapid changes in brain function.
Skin warts are benign tumours caused by infection of keratinocytes with HPV, visible as well‐defined hyperkeratotic protrusions. We will explore the detailed types, presentation, and treatment modalities of most common warts.
Journal Club: Prophylactic Thyroidectomy in Multiple Endocrine Neoplasia 2 Dr. Aryan (Anish Dhakal)
The study aims to analyze the long-term results of a large cohort of MEN2 patients with the C634Y mutation who had undergone prophylactic thyroidectomy in a tertiary referral hospital, and to analyze the results in terms of age and calcitonin levels.
Surgery Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan Part...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Pediatrics Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan P...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Medicine Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan Par...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Gynaecology and Obstetrics Review Booklet by Dr. Aryan (Medical Booklet Serie...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Radiology Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan Pa...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Ophthalmology Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Arya...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Forensic Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan Par...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
ENT Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan Part 12)Dr. Aryan (Anish Dhakal)
This document is a preface and introduction to a study material on ear, nose and throat disorders created by Dr. Aryan. It outlines that the material aims to provide a concise review of key information through slides with minimal relation between slides. It is meant as a high-yield review and recommends referring to textbooks for more comprehensive understanding. The preface emphasizes executing on knowledge gained and includes motivational quotes throughout. It is signed off by the creator, Dr. Aryan, wishing readers best of luck and success in their work.
Dentistry Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan Pa...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Dermatology Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan ...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Anaesthesia Review Booklet by Dr. Aryan (Medical Booklet Series by Dr. Aryan ...Dr. Aryan (Anish Dhakal)
This is a part of free booklet series designed by Dr. Aryan for rapid review of basic concepts of medical science. I grant you right to share the booklet for fair use (teaching, scholarship, education and research) anywhere in the world exclusively for non-monetary purposes.
Management of hypertensive condition in 2020 according to AHA/ASA guidelines. We will discuss the presentation, clinical assessment, investigations, and management of hypertension along with major randomized controlled trials and guidelines.
Redesigning Education as a Cognitive Ecosystem: Practical Insights into Emerg...Leonel Morgado
Slides used at the Invited Talk at the Harvard - Education University of Hong Kong - Stanford Joint Symposium, "Emerging Technologies and Future Talents", 2025-05-10, Hong Kong, China.
Rock Art As a Source of Ancient Indian HistoryVirag Sontakke
This Presentation is prepared for Graduate Students. A presentation that provides basic information about the topic. Students should seek further information from the recommended books and articles. This presentation is only for students and purely for academic purposes. I took/copied the pictures/maps included in the presentation are from the internet. The presenter is thankful to them and herewith courtesy is given to all. This presentation is only for academic purposes.
This chapter provides an in-depth overview of the viscosity of macromolecules, an essential concept in biophysics and medical sciences, especially in understanding fluid behavior like blood flow in the human body.
Key concepts covered include:
✅ Definition and Types of Viscosity: Dynamic vs. Kinematic viscosity, cohesion, and adhesion.
⚙️ Methods of Measuring Viscosity:
Rotary Viscometer
Vibrational Viscometer
Falling Object Method
Capillary Viscometer
🌡️ Factors Affecting Viscosity: Temperature, composition, flow rate.
🩺 Clinical Relevance: Impact of blood viscosity in cardiovascular health.
🌊 Fluid Dynamics: Laminar vs. turbulent flow, Reynolds number.
🔬 Extension Techniques:
Chromatography (adsorption, partition, TLC, etc.)
Electrophoresis (protein/DNA separation)
Sedimentation and Centrifugation methods.
What makes space feel generous, and how architecture address this generosity in terms of atmosphere, metrics, and the implications of its scale? This edition of #Untagged explores these and other questions in its presentation of the 2024 edition of the Master in Collective Housing. The Master of Architecture in Collective Housing, MCH, is a postgraduate full-time international professional program of advanced architecture design in collective housing presented by Universidad Politécnica of Madrid (UPM) and Swiss Federal Institute of Technology (ETH).
Yearbook MCH 2024. Master in Advanced Studies in Collective Housing UPM - ETH
What is the Philosophy of Statistics? (and how I was drawn to it)jemille6
What is the Philosophy of Statistics? (and how I was drawn to it)
Deborah G Mayo
At Dept of Philosophy, Virginia Tech
April 30, 2025
ABSTRACT: I give an introductory discussion of two key philosophical controversies in statistics in relation to today’s "replication crisis" in science: the role of probability, and the nature of evidence, in error-prone inference. I begin with a simple principle: We don’t have evidence for a claim C if little, if anything, has been done that would have found C false (or specifically flawed), even if it is. Along the way, I’ll sprinkle in some autobiographical reflections.
Form View Attributes in Odoo 18 - Odoo SlidesCeline George
Odoo is a versatile and powerful open-source business management software, allows users to customize their interfaces for an enhanced user experience. A key element of this customization is the utilization of Form View attributes.
How to Manage Purchase Alternatives in Odoo 18Celine George
Managing purchase alternatives is crucial for ensuring a smooth and cost-effective procurement process. Odoo 18 provides robust tools to handle alternative vendors and products, enabling businesses to maintain flexibility and mitigate supply chain disruptions.
Link your Lead Opportunities into Spreadsheet using odoo CRMCeline George
In Odoo 17 CRM, linking leads and opportunities to a spreadsheet can be done by exporting data or using Odoo’s built-in spreadsheet integration. To export, navigate to the CRM app, filter and select the relevant records, and then export the data in formats like CSV or XLSX, which can be opened in external spreadsheet tools such as Excel or Google Sheets.
How to Configure Public Holidays & Mandatory Days in Odoo 18Celine George
In this slide, we’ll explore the steps to set up and manage Public Holidays and Mandatory Days in Odoo 18 effectively. Managing Public Holidays and Mandatory Days is essential for maintaining an organized and compliant work schedule in any organization.
The insect cuticle is a tough, external exoskeleton composed of chitin and proteins, providing protection and support. However, as insects grow, they need to shed this cuticle periodically through a process called moulting. During moulting, a new cuticle is prepared underneath, and the old one is shed, allowing the insect to grow, repair damaged cuticle, and change form. This process is crucial for insect development and growth, enabling them to transition from one stage to another, such as from larva to pupa or adult.
Ancient Stone Sculptures of India: As a Source of Indian HistoryVirag Sontakke
This Presentation is prepared for Graduate Students. A presentation that provides basic information about the topic. Students should seek further information from the recommended books and articles. This presentation is only for students and purely for academic purposes. I took/copied the pictures/maps included in the presentation are from the internet. The presenter is thankful to them and herewith courtesy is given to all. This presentation is only for academic purposes.
How to Add Customer Note in Odoo 18 POS - Odoo SlidesCeline George
In this slide, we’ll discuss on how to add customer note in Odoo 18 POS module. Customer Notes in Odoo 18 POS allow you to add specific instructions or information related to individual order lines or the entire order.
Happy May and Happy Weekend, My Guest Students.
Weekends seem more popular for Workshop Class Days lol.
These Presentations are timeless. Tune in anytime, any weekend.
<<I am Adult EDU Vocational, Ordained, Certified and Experienced. Course genres are personal development for holistic health, healing, and self care. I am also skilled in Health Sciences. However; I am not coaching at this time.>>
A 5th FREE WORKSHOP/ Daily Living.
Our Sponsor / Learning On Alison:
Sponsor: Learning On Alison:
— We believe that empowering yourself shouldn’t just be rewarding, but also really simple (and free). That’s why your journey from clicking on a course you want to take to completing it and getting a certificate takes only 6 steps.
Hopefully Before Summer, We can add our courses to the teacher/creator section. It's all within project management and preps right now. So wish us luck.
Check our Website for more info: https://ldmchapels.weebly.com
Get started for Free.
Currency is Euro. Courses can be free unlimited. Only pay for your diploma. See Website for xtra assistance.
Make sure to convert your cash. Online Wallets do vary. I keep my transactions safe as possible. I do prefer PayPal Biz. (See Site for more info.)
Understanding Vibrations
If not experienced, it may seem weird understanding vibes? We start small and by accident. Usually, we learn about vibrations within social. Examples are: That bad vibe you felt. Also, that good feeling you had. These are common situations we often have naturally. We chit chat about it then let it go. However; those are called vibes using your instincts. Then, your senses are called your intuition. We all can develop the gift of intuition and using energy awareness.
Energy Healing
First, Energy healing is universal. This is also true for Reiki as an art and rehab resource. Within the Health Sciences, Rehab has changed dramatically. The term is now very flexible.
Reiki alone, expanded tremendously during the past 3 years. Distant healing is almost more popular than one-on-one sessions? It’s not a replacement by all means. However, its now easier access online vs local sessions. This does break limit barriers providing instant comfort.
Practice Poses
You can stand within mountain pose Tadasana to get started.
Also, you can start within a lotus Sitting Position to begin a session.
There’s no wrong or right way. Maybe if you are rushing, that’s incorrect lol. The key is being comfortable, calm, at peace. This begins any session.
Also using props like candles, incenses, even going outdoors for fresh air.
(See Presentation for all sections, THX)
Clearing Karma, Letting go.
Now, that you understand more about energies, vibrations, the practice fusions, let’s go deeper. I wanted to make sure you all were comfortable. These sessions are for all levels from beginner to review.
Again See the presentation slides, Thx.
2. Preface:
This is the study material designed by Aryan with the sole purpose of revising
and simplifying concepts in biostatistics which many students find difficult and
overwhelming.
Covering everything in one study material is next to impossible. Hence, refer to
gold standard textbooks for building solid concepts or in case of any doubt.
Don’t keep searching for pattern between the consecutive slides. You won’t find
many. Rather to boost your recall and review, I have constructed slides and are
deliberately placed with no much relation between the preceding and the
succeeding ones.
The main rule of a review material is that it must make you recall or learn
maximum amount of information in minimum amount of time and space.
Always remember, everything is literally and absolutely worthless unless you do.
If you know everything in the slides in much detail, you probably wouldn’t need
this material.
Best of luck WORK & SUCCESS! Anish Dhakal (Aryan)
3. 21 Concepts to Master:
1. Normal distribution
2. Skewness
3. Kurtosis
4. Sampling distribution of sample means
5. Central limit theorem
6. Z-score
7. Margin of error
8. Minimum sample size
9. Hypothesis testing
10. p value
11. Critical value
12. , Z-scores, Critical region & Area
under the curve
13. Statement of acceptance or rejection
of claims
14. Probability
15. Binomial and Multinomial probability
16. Discrete probability distribution
17. Fundamental of counting rule
18. Poisson distribution
19. Correlation & Regression
20. Line of best fit
21. Coefficient of determination
4. Normal Distribution
This is the standard normal bell
shaped curve.
Features of distribution
a) Continuous
b) Symmetric
c) Bell-shaped
Mean is Zero (0) and Standard
Deviation is One (1)
Total area: 1.00 or 100%
Anish Dhakal (Aryan)
5. Chebyshev’s theorem gives the
formula 1-1/k2
That is for any distribution of
data.
In normal distribution, more
data is concentrated. For
example, the theorem states 75%
of data within 2 S.D. In normal
curve, the number is above 95%
Anish Dhakal (Aryan)
6. Skewness
If data is perfectly
symmetrical, skewness= Zero
Positive skewness: Right side
of the curve is longer or fatter
(Mean>Median>Mode). As you
can see majority of data is on
the right side: Right skewed)
Negative skewness: Left side
of the curve is longer or fatter
(Mean<Median<Mode). As you
can see majority of data is on
left side: Left skewed)
Anish Dhakal (Aryan)
8. Distribution of Sample Means
Samples are vital as we cannot go and measure the data from large
population every time.
Now, let’s take many random samples from one population each of
size “n”.
Calculate mean of all the samples taken from that population.
Now calculate the mean of all the mean of the samples.
That’s exactly what sampling distribution of sample means is all
about.
Anish Dhakal (Aryan)
9. Distribution of Sample Means (taken
with replacement)
I. Mean will be same as population mean (µ)
II. Standard Deviation of Sample (from mean)
= Standard error of mean
= SD of population/ 𝑁𝑜. 𝑜𝑓 𝑠𝑎𝑚𝑝𝑙𝑒𝑠
= σ/ 𝒏
Anish Dhakal (Aryan)
10. Central Limit Theorem
When sample size “n” increases without limit, the distribution of
sample means approaches the normal distribution.
If original population is not normally distributed, we need n≥30.
If sample size is less than 30, population must be already normally
distributed.
Anish Dhakal (Aryan)
12. Confidence Interval of 90%, 95% & 99%
Remember the Critical Value Numbers (two-tailed tests):
90%: 1.65
95%: 1.96
99%: 2.58
Anish Dhakal (Aryan)
13. Margin of Error
Formula for Interval: ഥ𝑿- Z (σ/√𝒏) < µ < ഥ𝑿 + Z (σ/√𝒏)
If population standard deviation (σ) is not known, use t values and S (standard
deviation of sample). In such cases, n-1 would be the degree of freedom. As degree
of freedom increases further, t distribution would approach normal distribution
among many family of curves with discrete degrees of freedom.
Here, Z (σ/√𝑛) is the margin of error or maximum error of estimate
Maximum error of estimate (E) = Z (σ/√𝒏)
= Z
𝒑𝒒
𝒏
(Margin of error while using proportions)
Anish Dhakal (Aryan)
14. Minimum Sample Size
n=
Z2 pq
E2 (for proportions)
n =
Z2σ2
E2
The same can also be deduced from the previous formula for margin
of error where,
E = Z (σ/√𝒏) or Z
𝒑𝒒
𝒏
Anish Dhakal (Aryan)
15. Null and Alternate Hypothesis
Null: H0: µ=k
Alternate: H1
I. H1: µ ≠ k (two-tailed test)
II. H1: µ > k (right-tailed test)
III. H1: µ < k (left-tailed test)
Null hypothesis Errors:
1) Reject when H0 true: Type I Error
2) Do not reject when H0 not true: Type II Error
Maximum probability of committing Type I Error (rejection of null hypothesis when it is true) is
equal to the level of significance (). Confidence level = 1-. 1-ß (ß being the Type II Error) is the
power of the test.
16. p value
p value denotes how much of your result can occur due to chance
(sampling error).
If the p value is less than the level of significance (), the
hypothesis test is statistically significant
In other words, if your p value is less than the , then your
confidence interval will not contain the null hypothesis value. Hence
you can safely reject the null hypothesis (value in critical or rejection
region).
Anish Dhakal (Aryan)
17. Confusion Corner: , Z-scores, Critical Region
& Area Under the Curve
The first aspect is to consider whether it is left, right or two-tailed
curve we are dealing with. If someone says you that the critical value
for 95% confidence interval is 1.96, it assumes that it is a two tailed
test (hence the notation Z /2 read as zee sub alpha over two).
When you get (in this case 0.025 on first point), that would give
the area of the curve that we are concerned about. By convention,
while you search for the nearest area in the body of z-table, it is area
to the left of the point. Look for corresponding z-scores (critical
values).
Alternatively, if you are given z-scores like in the figure alongside,
trace for the area in the table. The first point at -1.96 gives area
0.0250 (blue shaded area on left) and the point +1.96 gives area
0.9750 (blue shaded area on left + non-shaded area in middle).
The blue shaded area on the right also have area of 0.0250 (its same
as the left side only to be on positive side). If you need area of the
middle portion, that would be 0.9750 - 0.0250 = 0.9500 (95%
confidence level on a two-tailed test with critical region 2.5% on left
and 2.5% on right). Anish Dhakal (Aryan)
19. Traditional Z-Test for Hypothesis
Testing
1. State null hypothesis and identify the claim (null or alternate hypothesis)
2. Find the critical value (Z-value) on table with given (based on whether
it is left-tailed: critical value corresponding to , right-tailed: critical
value corresponding to 1- or two-tailed: critical value corresponding to
/2 and 1- /2 on left and right side respectively)
3. Compute the test value (Z-value)
4. Compare the critical value(s) and computed value in Step 2 & Step 3.
Make a decision about the location of computed value. Does the
computed value fall in the critical region or not? If it falls in critical
region, reject the null hypothesis. Note that here we are comparing z-
values based on and based on what we calculate. We cannot compare
the areas as that would be same for both positive and negative z-values.
20. P-value Test for Hypothesis Testing
1. State the hypothesis and identify the claim
2. Compute the test value (Z-value)
3. Find the p-value. Find value corresponding to z-value on the table
(area). If this is a left-tailed test, that corresponding value is your p-
value. If this is a right tailed test, you need to find the rightmost area
beyond the point of z value so use 1-corresponding value. If this is a
two-tailed test, your final p-value would be either double the
corresponding value or double of (1-corresponding value) depending
on whether your z-value is negative or positive respectively.
4. Now all you need to do is compare your p-value with the level of
significance (). On a 5% level of significance, reject null hypothesis
(the difference is significant) if p-value<0.05. If p-value is greater than
or equal to 0.05, there is not enough evidence to reject the null
hypothesis.
21. How to state the acceptance and rejection of
claims?
Claim is Ho (Null hypothesis):
A. Reject Ho: There is enough evidence to reject null hypothesis
B. Do not reject Ho: There is not enough evidence to reject null
hypothesis
Claim is H1 (Alternate Hypothesis):
A. Reject Ho: There is enough evidence to support alternate hypothesis
B. Do not reject Ho: There is not enough evidence to support alternate
hypothesis
Anish Dhakal (Aryan)
22. Concept of Hypothesis Testing
While you test a hypothesis, never simply say that null hypothesis is
true or false. You do not know that!
The only thing you know is that based on evidence provided, there is
enough evidence to reject the null hypothesis or not. To state with
100% certainty whether that is true or false, whole population needs
to be tested.
When a null hypothesis is rejected at a level of significance , the
confidence interval computed at 1- would not contain the value of
mean stated by the null hypothesis and vice versa. That’s pretty
obvious.
Anish Dhakal (Aryan)
23. Probability
Classical probability: all outcomes equally likely to happen (sample
spaces)
Empirical probability: actual experiments to determine probability
(frequency distribution)
Conditional probability: The probability that second event B occurs
given that the first event A has occurred can be found by:
P(B|A) = P(A and B)/P(A)
Anish Dhakal (Aryan)
24. Fundamental of Counting Rule
I. If repetitions are permitted, the numbers stay the same going from
left to right. For example if a number of 5 digits is to be selected
the total number of possibilities = 10*10*10*10*10 = 100000
possibilities of selecting a 5 digit number.
II. If repetitions are not permitted, we got one less choice every time.
The numbers decrease by one for each place left to right. Total
number of possibilities in the above example = 10*9*8*7*6 =
30240 possibilities of selecting a 5 digit number.
Anish Dhakal (Aryan)
25. Permutation and Combination
Permutation of ‘n’ objects taking ‘r’ objects at a time (in specific order):
𝒏 𝑷 𝒓 =
𝒏!
𝒏−𝒓 !
Combination of ‘r’ object selected from ‘n’ objects:
nCr =
𝒏!
𝒏−𝒓 !𝒓!
Hence, nCr = nPr
𝒓!
(r! removes the duplicates which have great
significance in permutation. 1 & 2 or 2 & 1 would be same in combination)
Anish Dhakal (Aryan)
26. Mean of random variable with discrete
probability distributions:
µ = X1.P(X1) + X2.P(X2) + ………………………………... + Xn.P(Xn) = Σ[X.P(X)]
where,
X1, X2……………….Xn are the outcomes
P(X1), P (X2)………P(Xn) are the corresponding probabilities
Anish Dhakal (Aryan)
27. Binomial Distribution of Probability
Condition for binomial probability experiment:
i. Fixed number of trials
ii. Two outcomes or results can be reduced to two outcomes
iii. Outcomes of each trial independent of each other
iv. Probability of success remains the same for each trial
P(x=k) = b(k; n,p) =
𝒏!
𝒏−𝒌 !𝒌!
.pk.qn-k = C(n,k).pk.qn-k
where,
p= probability of success
q= probability of failure
n= number of trials
k= number of success (at x=k) (0≤x≤n) Anish Dhakal (Aryan)
28. Multinomial Distribution
P(x) =
𝒏!
x1!x2!x3!....................xk!
. 𝐩1
x1.p2
x2……….pk
xk
where,
x1,x2,x3…………………..xk are number of occurrence of events
p1, p2, p3………………..pk are the corresponding probabilities
x1+x2+x3………………….xk= n (total number of events)
p1+p2+p3………………….pk = 1
Anish Dhakal (Aryan)
29. Poisson Distribution
P(x, λ)=
e−ʎ.ʎx
𝒙!
where,
ʎ= mean number of occurrence per unit time, length, area or volume
x= number of occurrence of the event
e= 2.7183
n: sufficiently large
probability of success: sufficiently small
Anish Dhakal (Aryan)
30. Correlation Vs. Regression
Correlation:
simply determines whether two variables are correlated and to what extent.
Regression:
determines nature of relationships, estimate dependent variable based on
independent variable (functional relationship/projection of events).
Anish Dhakal (Aryan)
31. Line of Best Fit
Choose a straight line which best represents the scatter plot and you
have got the line of best fit.
Sum of squares from each point to the line is minimum.
Equation of the line (Regression line equation):
Predicted value (y’)= a+bx
where,
a= y-intercept
x= slope of line
Closer the observed value (y) is to the predicted value (y’), the better is the
fit and the closer ‘r’ is to +1 or -1.
Anish Dhakal (Aryan)
32. Total variation = Explained variation + Unexplained variation
= Σ(y’-തy)2 + Σ(y-y’)2
= Σ(y-തy)2
y-y’ is the unexplained deviation or residuals. Sum of the square of residuals Σ(y-y’)2 being
the least possible value gives rise to line of best fit.
33. Coefficient of determination
r2 =
explained variation
total variation
=
Σ(y’−ഥy)2
Σ(y−ഥy)2
This is the percentage of total variation explained by the regression
line using the independent variable.
1-r2: coefficient of non-determination: due to chance
Anish Dhakal (Aryan)
34. Why we don’t like studying?
Visit: https://qr.ae/T9mWzf
Anish Dhakal (Aryan)