Mathematics in Epidemiology and Biostatistics (Medical Booklet Series by Dr. ...Dr. Aryan (Anish Dhakal)
Basic mathematics needed for epidemiology and bio statistics. Slides include formulas and conceptual understanding of sensitivity, specificity, predictive values, likelihood ratios, odds, probability and many more.
SAMPLE SIZE CALCULATION IN DIFFERENT STUDY DESIGNS AT.pptxssuserd509321
The document discusses factors that affect sample size calculation in different study designs. It provides examples of calculating sample sizes for descriptive cross-sectional studies, case-control studies, cohort studies, comparative studies, and randomized controlled trials. The key factors discussed are the level of confidence, power, expected proportions or means in groups, margin of error, and standard deviation. Sample size is affected by the type of study design, variables being qualitative or quantitative, and the goal of establishing equivalence, superiority or non-inferiority between groups. Electronic resources are provided for calculating sample sizes.
An epidemic curve (or epi curve) is a graphical depiction of the number of illness cases by date of onset that can help characterize outbreaks. The shape and features of the curve can reveal the pattern of spread (e.g. common source, point source, propagated), magnitude, outliers, time trends, and estimate the exposure period. Epi curves are useful for outbreak investigation and response.
The document discusses ROC (receiver operating characteristic) curves and their use in analyzing diagnostic tests. It provides three key points:
1) ROC curves plot the true positive rate against the false positive rate for a binary classifier system as its discrimination threshold is varied. This allows visualization of the classifier's performance.
2) Originally developed for military radar analysis, ROC curves differentiate signal from noise as classifier sensitivity increases and specificity decreases.
3) The document provides an example of using an ROC curve to evaluate chest radiography results for diagnosing malignant pulmonary nodules based on biopsy results, demonstrating calculation of sensitivity and specificity at different classification thresholds.
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.
Measures of association like the relative risk (RR) and odds ratio (OR) quantify the strength between an exposure and disease. An RR or OR of 1 means no association, above 1 means positive association, and below 1 means negative association. The RR compares outcomes between exposed and unexposed groups in cohort studies, while the OR provides an estimate of the RR using case-control studies. Confidence intervals describe the precision of a point estimate, with a narrower interval indicating a more precise estimate. Interpreting if a 95% CI includes 1 determines if there is a statistically significant association.
This document discusses case-control study design and calculating odds ratios. It provides examples of 3 case-control studies examining suspected risk factors for cervical cancer, lung cancer, and esophageal cancer. For each study, it constructs a 2x2 contingency table and calculates the odds ratio to assess the strength of association between the disease and suspected risk factor. Odds ratios greater than 1 indicate the exposure increases disease risk.
The ppt is a short description about how to ascertain the validity, ie; sensitivity and specificity of a screening test as well as their predictive powers. you can also find the technique to ascertain the best possible screening test through the help of an ROC curve...
The document is comprised of 21 lines that repeat the same phrase "Prof (Dr) C M Singh". It does not contain any other words or meaningful information, simply repeating the same phrase on each line.
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.
Sensitivity, specificity, positive and negative predictiveMusthafa Peedikayil
This document defines and provides formulas to calculate sensitivity, specificity, positive predictive value, and negative predictive value for medical tests. Sensitivity measures the percentage of true positives, or how well a test detects those with a disease. Specificity measures the percentage of true negatives, or how well a test identifies those without disease. Positive predictive value refers to the probability a patient has the disease given a positive test result. Negative predictive value refers to the probability a patient does not have the disease given a negative test result. Formulas are provided using a 2x2 contingency table to calculate each value.
Screening is a tool used to identify undiagnosed cases of disease in a population using rapid tests. The objectives of screening are to reduce mortality and morbidity through early detection and treatment, and to maintain or enhance production through better disease management. Screening aims to separate healthy individuals who likely have a disease from those who do not, though a positive screening test requires more diagnostic testing. Effective screening involves both diagnostic testing and treatment components, and aims to identify existing disease in asymptomatic individuals. The only valid measure of a screening program's effectiveness is its impact on disease-specific mortality rates.
Screening for diseases from community medicine. It explains the definition of screening, lead time, uses of screening, differences between screening and diagnostic test, criteria for a disease to be screened and criteria for a screening test, cut-off points, etc
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.
Incidence and prevalence measures provide information about disease frequency and burden in populations. Prevalence describes the proportion of people with a disease at a point in time, while incidence refers to the number of new cases that develop over time. Both measures can be stratified by person, place, and time to gain insights into a disease's pathogenesis and development.
The document discusses receiver operator characteristic (ROC) curves which assess the sensitivity and specificity of diagnostic tests. ROC curves plot the true positive rate against the false positive rate. Changing the cutoff value for a positive test result affects the sensitivity and specificity. A test with a curve closer to the upper left corner is more accurate. The area under the ROC curve (AUC) measures diagnostic efficacy, with a higher AUC indicating a better performing test. ROC curves can also compare the sensitivity and specificity of different diagnostic tests.
A 25-year-old man presented to the casualty ward with deep wounds on both legs from an injury the previous day. He had received the tetanus toxoid vaccine 12 years ago. The wounds were cleaned and sutured if necessary. Antibiotics were administered within 6 hours to prevent tetanus. The man also received a booster dose of the tetanus toxoid vaccine due to the long interval since his last dose to actively immunize against tetanus infection from the wounds.
This document discusses cohort studies. A cohort study compares outcomes between groups that differ in their exposure to a risk factor. It involves selecting groups of individuals, measuring their exposure to a risk factor, observing them for a defined outcome, and analyzing any association. The key elements are defining the study question, selecting and measuring exposure in study populations, following up to ascertain outcomes, and analyzing results like incidence rates and relative risks. Cohort studies provide strong evidence but require large sample sizes and long follow-up periods.
Secondary attack rates measure the spread of infection within a closed group exposed to a primary case, calculated as the number of secondary cases divided by the number of susceptible individuals excluding the primary case. They are used to evaluate disease spread within families and the effectiveness of control measures like isolation and immunization. Limitations include difficulty identifying susceptibles for diseases with subclinical cases and accounting for variable exposure durations.
This document provides an introduction to epidemiological studies. It defines epidemiology as the study of disease distributions in populations and factors that influence distribution. It describes the hierarchy of evidence in epidemiology, including descriptive and analytical studies. Descriptive studies like case reports and prevalence surveys describe disease patterns, while analytical studies test hypotheses. The main analytical study designs are cross-sectional studies, case-control studies, and prospective cohort studies. Each design differs in sampling, time orientation, and ability to infer causality. Cross-sectional studies measure prevalence, case-control studies infer causality retrospectively, and prospective cohort studies follow exposed groups over time to measure incidence.
ODDS RATIO AND RELATIVE RISK EVALUATIONKanhu Charan
Relative risk and odds ratio are measures used to quantify the strength of association between an exposure and an outcome. Relative risk is calculated as the incidence of an outcome in an exposed group divided by the incidence in an unexposed group. It is the preferred measure for cohort studies where the number of people at risk is known. Odds ratio is calculated as the odds of exposure in those with the outcome divided by the odds of exposure in those without the outcome. It is used for case-control studies where the total number exposed is not known. Both measures can help determine if a risk factor increases, decreases, or has no effect on the risk of an outcome. The key difference is that relative risk utilizes probabilities while odds ratio uses odds.
An independent samples t-test is used to compare two groups and is appropriate when the independent variable has two levels, while a one-way ANOVA can compare more than two groups and should be used when the independent variable has three or more levels. The document provides examples of when to use an independent samples t-test versus a one-way ANOVA based on whether the independent variable has two or more than two levels.
This document discusses survival analysis techniques. It begins with an overview of survival, censoring, and the need for survival analysis when not all patients have died or had the event of interest. It then describes the key techniques of life tables/actuarial analysis and the Kaplan-Meier method. Life tables involve constructing a hypothetical cohort and estimating survival at different ages based on mortality rates. The Kaplan-Meier method is commonly used to illustrate survival curves and gives partial credit to censored observations. A modified life table is also presented to analyze survival outcomes in different treatment groups.
These annotated slides will help you interpret an OR or RR in clinical terms. Please download these slides and view them in PowerPoint so you can view the annotations describing each slide.
This document discusses sample size estimation and the factors that influence determining an appropriate sample size for research studies. It provides examples of calculating sample sizes based on prevalence of a disease, mean values, standard deviations, permissible errors, and confidence levels. The key points are:
- Sample size depends on prevalence/magnitude of the attribute being studied, permissible error, and power of the statistical test
- Larger sample sizes are needed to detect smaller differences and have sufficient power
- Examples are provided to demonstrate calculating sample sizes based on prevalence of anemia, mean blood pressure values, and acceptable margins of error
Attributable risk and population attributable riskAbino David
This document defines risk factors and describes methods for identifying and quantifying risk. It defines a risk factor as an attribute or exposure associated with disease development. Epidemiological studies help identify risk factors and estimate degree of risk. Relative risk compares incidence between exposed and unexposed groups, while attributable risk indicates how much disease can be attributed to exposure by comparing incidence rates. Two examples are given to illustrate these concepts and how attributable risk informs potential public health interventions.
The document discusses various measures used to assess the strength and nature of associations between variables in epidemiological studies. It describes difference measures like absolute risk and ratio measures like relative risk and odds ratio. It explains how relative risk is calculated in cohort studies and how odds ratio is used as a measure of association in case-control studies. The relationship between relative risk and odds ratio is also covered.
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.
The document is comprised of 21 lines that repeat the same phrase "Prof (Dr) C M Singh". It does not contain any other words or meaningful information, simply repeating the same phrase on each line.
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.
Sensitivity, specificity, positive and negative predictiveMusthafa Peedikayil
This document defines and provides formulas to calculate sensitivity, specificity, positive predictive value, and negative predictive value for medical tests. Sensitivity measures the percentage of true positives, or how well a test detects those with a disease. Specificity measures the percentage of true negatives, or how well a test identifies those without disease. Positive predictive value refers to the probability a patient has the disease given a positive test result. Negative predictive value refers to the probability a patient does not have the disease given a negative test result. Formulas are provided using a 2x2 contingency table to calculate each value.
Screening is a tool used to identify undiagnosed cases of disease in a population using rapid tests. The objectives of screening are to reduce mortality and morbidity through early detection and treatment, and to maintain or enhance production through better disease management. Screening aims to separate healthy individuals who likely have a disease from those who do not, though a positive screening test requires more diagnostic testing. Effective screening involves both diagnostic testing and treatment components, and aims to identify existing disease in asymptomatic individuals. The only valid measure of a screening program's effectiveness is its impact on disease-specific mortality rates.
Screening for diseases from community medicine. It explains the definition of screening, lead time, uses of screening, differences between screening and diagnostic test, criteria for a disease to be screened and criteria for a screening test, cut-off points, etc
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.
Incidence and prevalence measures provide information about disease frequency and burden in populations. Prevalence describes the proportion of people with a disease at a point in time, while incidence refers to the number of new cases that develop over time. Both measures can be stratified by person, place, and time to gain insights into a disease's pathogenesis and development.
The document discusses receiver operator characteristic (ROC) curves which assess the sensitivity and specificity of diagnostic tests. ROC curves plot the true positive rate against the false positive rate. Changing the cutoff value for a positive test result affects the sensitivity and specificity. A test with a curve closer to the upper left corner is more accurate. The area under the ROC curve (AUC) measures diagnostic efficacy, with a higher AUC indicating a better performing test. ROC curves can also compare the sensitivity and specificity of different diagnostic tests.
A 25-year-old man presented to the casualty ward with deep wounds on both legs from an injury the previous day. He had received the tetanus toxoid vaccine 12 years ago. The wounds were cleaned and sutured if necessary. Antibiotics were administered within 6 hours to prevent tetanus. The man also received a booster dose of the tetanus toxoid vaccine due to the long interval since his last dose to actively immunize against tetanus infection from the wounds.
This document discusses cohort studies. A cohort study compares outcomes between groups that differ in their exposure to a risk factor. It involves selecting groups of individuals, measuring their exposure to a risk factor, observing them for a defined outcome, and analyzing any association. The key elements are defining the study question, selecting and measuring exposure in study populations, following up to ascertain outcomes, and analyzing results like incidence rates and relative risks. Cohort studies provide strong evidence but require large sample sizes and long follow-up periods.
Secondary attack rates measure the spread of infection within a closed group exposed to a primary case, calculated as the number of secondary cases divided by the number of susceptible individuals excluding the primary case. They are used to evaluate disease spread within families and the effectiveness of control measures like isolation and immunization. Limitations include difficulty identifying susceptibles for diseases with subclinical cases and accounting for variable exposure durations.
This document provides an introduction to epidemiological studies. It defines epidemiology as the study of disease distributions in populations and factors that influence distribution. It describes the hierarchy of evidence in epidemiology, including descriptive and analytical studies. Descriptive studies like case reports and prevalence surveys describe disease patterns, while analytical studies test hypotheses. The main analytical study designs are cross-sectional studies, case-control studies, and prospective cohort studies. Each design differs in sampling, time orientation, and ability to infer causality. Cross-sectional studies measure prevalence, case-control studies infer causality retrospectively, and prospective cohort studies follow exposed groups over time to measure incidence.
ODDS RATIO AND RELATIVE RISK EVALUATIONKanhu Charan
Relative risk and odds ratio are measures used to quantify the strength of association between an exposure and an outcome. Relative risk is calculated as the incidence of an outcome in an exposed group divided by the incidence in an unexposed group. It is the preferred measure for cohort studies where the number of people at risk is known. Odds ratio is calculated as the odds of exposure in those with the outcome divided by the odds of exposure in those without the outcome. It is used for case-control studies where the total number exposed is not known. Both measures can help determine if a risk factor increases, decreases, or has no effect on the risk of an outcome. The key difference is that relative risk utilizes probabilities while odds ratio uses odds.
An independent samples t-test is used to compare two groups and is appropriate when the independent variable has two levels, while a one-way ANOVA can compare more than two groups and should be used when the independent variable has three or more levels. The document provides examples of when to use an independent samples t-test versus a one-way ANOVA based on whether the independent variable has two or more than two levels.
This document discusses survival analysis techniques. It begins with an overview of survival, censoring, and the need for survival analysis when not all patients have died or had the event of interest. It then describes the key techniques of life tables/actuarial analysis and the Kaplan-Meier method. Life tables involve constructing a hypothetical cohort and estimating survival at different ages based on mortality rates. The Kaplan-Meier method is commonly used to illustrate survival curves and gives partial credit to censored observations. A modified life table is also presented to analyze survival outcomes in different treatment groups.
These annotated slides will help you interpret an OR or RR in clinical terms. Please download these slides and view them in PowerPoint so you can view the annotations describing each slide.
This document discusses sample size estimation and the factors that influence determining an appropriate sample size for research studies. It provides examples of calculating sample sizes based on prevalence of a disease, mean values, standard deviations, permissible errors, and confidence levels. The key points are:
- Sample size depends on prevalence/magnitude of the attribute being studied, permissible error, and power of the statistical test
- Larger sample sizes are needed to detect smaller differences and have sufficient power
- Examples are provided to demonstrate calculating sample sizes based on prevalence of anemia, mean blood pressure values, and acceptable margins of error
Attributable risk and population attributable riskAbino David
This document defines risk factors and describes methods for identifying and quantifying risk. It defines a risk factor as an attribute or exposure associated with disease development. Epidemiological studies help identify risk factors and estimate degree of risk. Relative risk compares incidence between exposed and unexposed groups, while attributable risk indicates how much disease can be attributed to exposure by comparing incidence rates. Two examples are given to illustrate these concepts and how attributable risk informs potential public health interventions.
The document discusses various measures used to assess the strength and nature of associations between variables in epidemiological studies. It describes difference measures like absolute risk and ratio measures like relative risk and odds ratio. It explains how relative risk is calculated in cohort studies and how odds ratio is used as a measure of association in case-control studies. The relationship between relative risk and odds ratio is also covered.
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.
K12 Tableau Tuesday - Algebra Equity and Access in Atlanta Public Schoolsdogden2
Algebra 1 is often described as a “gateway” class, a pivotal moment that can shape the rest of a student’s K–12 education. Early access is key: successfully completing Algebra 1 in middle school allows students to complete advanced math and science coursework in high school, which research shows lead to higher wages and lower rates of unemployment in adulthood.
Learn how The Atlanta Public Schools is using their data to create a more equitable enrollment in middle school Algebra classes.
How to Subscribe Newsletter From Odoo 18 WebsiteCeline George
Newsletter is a powerful tool that effectively manage the email marketing . It allows us to send professional looking HTML formatted emails. Under the Mailing Lists in Email Marketing we can find all the Newsletter.
Exploring Substances:
Acidic, Basic, and
Neutral
Welcome to the fascinating world of acids and bases! Join siblings Ashwin and
Keerthi as they explore the colorful world of substances at their school's
National Science Day fair. Their adventure begins with a mysterious white paper
that reveals hidden messages when sprayed with a special liquid.
In this presentation, we'll discover how different substances can be classified as
acidic, basic, or neutral. We'll explore natural indicators like litmus, red rose
extract, and turmeric that help us identify these substances through color
changes. We'll also learn about neutralization reactions and their applications in
our daily lives.
by sandeep swamy
Geography Sem II Unit 1C Correlation of Geography with other school subjectsProfDrShaikhImran
The correlation of school subjects refers to the interconnectedness and mutual reinforcement between different academic disciplines. This concept highlights how knowledge and skills in one subject can support, enhance, or overlap with learning in another. Recognizing these correlations helps in creating a more holistic and meaningful educational experience.
The Pala kings were people-protectors. In fact, Gopal was elected to the throne only to end Matsya Nyaya. Bhagalpur Abhiledh states that Dharmapala imposed only fair taxes on the people. Rampala abolished the unjust taxes imposed by Bhima. The Pala rulers were lovers of learning. Vikramshila University was established by Dharmapala. He opened 50 other learning centers. A famous Buddhist scholar named Haribhadra was to be present in his court. Devpala appointed another Buddhist scholar named Veerdeva as the vice president of Nalanda Vihar. Among other scholars of this period, Sandhyakar Nandi, Chakrapani Dutta and Vajradatta are especially famous. Sandhyakar Nandi wrote the famous poem of this period 'Ramcharit'.
Odoo Inventory Rules and Routes v17 - Odoo SlidesCeline George
Odoo's inventory management system is highly flexible and powerful, allowing businesses to efficiently manage their stock operations through the use of Rules and Routes.
A measles outbreak originating in West Texas has been linked to confirmed cases in New Mexico, with additional cases reported in Oklahoma and Kansas. The current case count is 817 from Texas, New Mexico, Oklahoma, and Kansas. 97 individuals have required hospitalization, and 3 deaths, 2 children in Texas and one adult in New Mexico. These fatalities mark the first measles-related deaths in the United States since 2015 and the first pediatric measles death since 2003.
The YSPH Virtual Medical Operations Center Briefs (VMOC) were created as a service-learning project by faculty and graduate students at the Yale School of Public Health in response to the 2010 Haiti Earthquake. Each year, the VMOC Briefs are produced by students enrolled in Environmental Health Science Course 581 - Public Health Emergencies: Disaster Planning and Response. These briefs compile diverse information sources – including status reports, maps, news articles, and web content– into a single, easily digestible document that can be widely shared and used interactively. Key features of this report include:
- Comprehensive Overview: Provides situation updates, maps, relevant news, and web resources.
- Accessibility: Designed for easy reading, wide distribution, and interactive use.
- Collaboration: The “unlocked" format enables other responders to share, copy, and adapt seamlessly. The students learn by doing, quickly discovering how and where to find critical information and presenting it in an easily understood manner.
CURRENT CASE COUNT: 817 (As of 05/3/2025)
• Texas: 688 (+20)(62% of these cases are in Gaines County).
• New Mexico: 67 (+1 )(92.4% of the cases are from Eddy County)
• Oklahoma: 16 (+1)
• Kansas: 46 (32% of the cases are from Gray County)
HOSPITALIZATIONS: 97 (+2)
• Texas: 89 (+2) - This is 13.02% of all TX cases.
• New Mexico: 7 - This is 10.6% of all NM cases.
• Kansas: 1 - This is 2.7% of all KS cases.
DEATHS: 3
• Texas: 2 – This is 0.31% of all cases
• New Mexico: 1 – This is 1.54% of all cases
US NATIONAL CASE COUNT: 967 (Confirmed and suspected):
INTERNATIONAL SPREAD (As of 4/2/2025)
• Mexico – 865 (+58)
‒Chihuahua, Mexico: 844 (+58) cases, 3 hospitalizations, 1 fatality
• Canada: 1531 (+270) (This reflects Ontario's Outbreak, which began 11/24)
‒Ontario, Canada – 1243 (+223) cases, 84 hospitalizations.
• Europe: 6,814
CBSE - Grade 8 - Science - Chemistry - Metals and Non Metals - WorksheetSritoma Majumder
Introduction
All the materials around us are made up of elements. These elements can be broadly divided into two major groups:
Metals
Non-Metals
Each group has its own unique physical and chemical properties. Let's understand them one by one.
Physical Properties
1. Appearance
Metals: Shiny (lustrous). Example: gold, silver, copper.
Non-metals: Dull appearance (except iodine, which is shiny).
2. Hardness
Metals: Generally hard. Example: iron.
Non-metals: Usually soft (except diamond, a form of carbon, which is very hard).
3. State
Metals: Mostly solids at room temperature (except mercury, which is a liquid).
Non-metals: Can be solids, liquids, or gases. Example: oxygen (gas), bromine (liquid), sulphur (solid).
4. Malleability
Metals: Can be hammered into thin sheets (malleable).
Non-metals: Not malleable. They break when hammered (brittle).
5. Ductility
Metals: Can be drawn into wires (ductile).
Non-metals: Not ductile.
6. Conductivity
Metals: Good conductors of heat and electricity.
Non-metals: Poor conductors (except graphite, which is a good conductor).
7. Sonorous Nature
Metals: Produce a ringing sound when struck.
Non-metals: Do not produce sound.
Chemical Properties
1. Reaction with Oxygen
Metals react with oxygen to form metal oxides.
These metal oxides are usually basic.
Non-metals react with oxygen to form non-metallic oxides.
These oxides are usually acidic.
2. Reaction with Water
Metals:
Some react vigorously (e.g., sodium).
Some react slowly (e.g., iron).
Some do not react at all (e.g., gold, silver).
Non-metals: Generally do not react with water.
3. Reaction with Acids
Metals react with acids to produce salt and hydrogen gas.
Non-metals: Do not react with acids.
4. Reaction with Bases
Some non-metals react with bases to form salts, but this is rare.
Metals generally do not react with bases directly (except amphoteric metals like aluminum and zinc).
Displacement Reaction
More reactive metals can displace less reactive metals from their salt solutions.
Uses of Metals
Iron: Making machines, tools, and buildings.
Aluminum: Used in aircraft, utensils.
Copper: Electrical wires.
Gold and Silver: Jewelry.
Zinc: Coating iron to prevent rusting (galvanization).
Uses of Non-Metals
Oxygen: Breathing.
Nitrogen: Fertilizers.
Chlorine: Water purification.
Carbon: Fuel (coal), steel-making (coke).
Iodine: Medicines.
Alloys
An alloy is a mixture of metals or a metal with a non-metal.
Alloys have improved properties like strength, resistance to rusting.
*Metamorphosis* is a biological process where an animal undergoes a dramatic transformation from a juvenile or larval stage to a adult stage, often involving significant changes in form and structure. This process is commonly seen in insects, amphibians, and some other animals.
A measles outbreak originating in West Texas has been linked to confirmed cases in New Mexico, with additional cases reported in Oklahoma and Kansas. The current case count is 795 from Texas, New Mexico, Oklahoma, and Kansas. 95 individuals have required hospitalization, and 3 deaths, 2 children in Texas and one adult in New Mexico. These fatalities mark the first measles-related deaths in the United States since 2015 and the first pediatric measles death since 2003.
The YSPH Virtual Medical Operations Center Briefs (VMOC) were created as a service-learning project by faculty and graduate students at the Yale School of Public Health in response to the 2010 Haiti Earthquake. Each year, the VMOC Briefs are produced by students enrolled in Environmental Health Science Course 581 - Public Health Emergencies: Disaster Planning and Response. These briefs compile diverse information sources – including status reports, maps, news articles, and web content– into a single, easily digestible document that can be widely shared and used interactively. Key features of this report include:
- Comprehensive Overview: Provides situation updates, maps, relevant news, and web resources.
- Accessibility: Designed for easy reading, wide distribution, and interactive use.
- Collaboration: The “unlocked" format enables other responders to share, copy, and adapt seamlessly. The students learn by doing, quickly discovering how and where to find critical information and presenting it in an easily understood manner.
How to manage Multiple Warehouses for multiple floors in odoo point of saleCeline George
The need for multiple warehouses and effective inventory management is crucial for companies aiming to optimize their operations, enhance customer satisfaction, and maintain a competitive edge.
Ultimate VMware 2V0-11.25 Exam Dumps for Exam SuccessMark Soia
Boost your chances of passing the 2V0-11.25 exam with CertsExpert reliable exam dumps. Prepare effectively and ace the VMware certification on your first try
Quality dumps. Trusted results. — Visit CertsExpert Now: https://www.certsexpert.com/2V0-11.25-pdf-questions.html
World war-1(Causes & impacts at a glance) PPT by Simanchala Sarab(BABed,sem-4...larencebapu132
This is short and accurate description of World war-1 (1914-18)
It can give you the perfect factual conceptual clarity on the great war
Regards Simanchala Sarab
Student of BABed(ITEP, Secondary stage)in History at Guru Nanak Dev University Amritsar Punjab 🙏🙏
Social Problem-Unemployment .pptx notes for Physiotherapy StudentsDrNidhiAgarwal
Unemployment is a major social problem, by which not only rural population have suffered but also urban population are suffered while they are literate having good qualification.The evil consequences like poverty, frustration, revolution
result in crimes and social disorganization. Therefore, it is
necessary that all efforts be made to have maximum.
employment facilities. The Government of India has already
announced that the question of payment of unemployment
allowance cannot be considered in India
How to track Cost and Revenue using Analytic Accounts in odoo Accounting, App...Celine George
Analytic accounts are used to track and manage financial transactions related to specific projects, departments, or business units. They provide detailed insights into costs and revenues at a granular level, independent of the main accounting system. This helps to better understand profitability, performance, and resource allocation, making it easier to make informed financial decisions and strategic planning.
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.
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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)
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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)
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