8.1 – The null and alternative hypotheses

Introduction

Classical statistical parametric tests — t-test (one sample t-test, independent sample-t-test), analysis of variance (ANOVA), correlation, and linear regression— and nonparametric tests like  (chi-square: goodness of fit and contingency table),  share several features that we need to understand. It’s natural to see all the details as if they are specific to each test, but there’s a theme that binds all of the classical statistical inference in order to make  claim of “statistical significance.”

• a calculated test statistic
• degrees of freedom associated with the calculation of the test statistic
• a probability value or p-value which is associated with the test statistic, assuming a null hypothesis is “true” in the population from which we sample.
  • Recall from our previous discussion (Chapter 8.2) that this is not strictly the interpretation of p-value, but a short-hand for how likely the data fit the null hypothesis. P-value alone can’t tell us about “truth.”
• in the event we reject the null hypothesis, we provisionally accept the alternative hypothesis.

Statistical Inference in the NHST Framework

By inference we mean to imply some formal process by which a conclusion is reached from data analysis of outcomes of an experiment. The process at its best leads to conclusions based on evidence. In statistics, evidence comes about from the careful and reasoned application of statistical procedures and the evaluation of probability (Abelson 1995).

Formally, statistics is rich in inference process (Bzdok et al, 2018). We begin by defining the classical frequentist, aka Neyman-Pearson approach, to inference, which involves the pairing of two kinds of statistical hypotheses: the null hypothesis (H_O) and the alternative hypothesis (H_A). The null hypothesis assumes that any observed difference between the groups are the results of random chance (introduced in Ch 2.3 – A brief history of (bio)statistics ), where “random chance” implies that outcomes occur without order or pattern (Eagle 2021). Whether we reject or accept the null hypothesis — a short-hand for the more appropriate “provisionally reject” in light of the humility that our results may reflect a rare sampling event — based on the outcome of our statistical inference, the inference is evaluated against a decision criterion (cf discussion in Christiansen 2005), a fixed statistical significance level (Lehmann 1992). Significance level refers to the setting of a p-value threshold before testing is done. The threshold is often set to Type I error of 5% (Cowles & Davis 1982), but researchers should always consider whether this threshold is appropriate for their work (Benjamin et al 2017).

This inference process is referred to as Null Hypothesis Significance Testing, NHST. Additionally, a probability value will be obtained for the test outcome or test statistic value. In the Fisherian likelihood tradition, the magnitude of this statistic value can be associated with a probability value, the p-value, of how likely the result is given the null hypothesis is “true.” (Again, keep in mind that this is not strictly the interpretation of p-value, it’s a short-hand for how likely the data fit the null hypothesis. P-value alone can’t tell us about “truth”, per our discussion, Chapter 8.2.)

-1*log(0.000134,10)
[1] 3.872895

> 10^(-1*3.872895)
[1] 0.0001340001

NHST Workflow

We presented in the introduction to Chapter 8 without discussion a simple flow chart to illustrate the process of decision (Fig 1, Chapter 8). Here, we repeat the flow chart diagram and follow with descriptions of the elements.

Figure 1. Flow chart of inductive statistical reasoning.

What’s missing from the flow chart is the very necessary caveat that interpretation of the null hypothesis is associated with two kinds of error, Type I error and Type II error. These points and others are discussed in the following sections.

We start with the hypothesis statements. For illustration we discuss hypotheses in terms of comparisons involving just two groups, also called two sample tests. One sample tests in contrast refer to scenarios where you compare a sample statistic to a population value. Extending these concepts to more than two samples is straightforward, but we leave that discussion to Chapters 12 – 18.

Null hypothesis

By far the most common application of the null hypothesis testing paradigm involves the comparisons of different treatment groups on some outcome variable. These kinds of null hypotheses are the subject of Chapters 8 through 12.

The Null hypothesis (H_O) is a statement about the comparisons, eg, between a sample statistic and the population, or between two treatment groups. The former is referred to as a one tailed test whereas the latter is called a two-tailed test. The null hypothesis is typically “no statistical difference” between the comparisons.

For example, a one sample, two tailed null hypothesis.

and we read it as “there is no statistical difference between our sample mean and the population mean.” For the more likely case in which no population mean is available, we provide another example, a two sample, two tailed null hypothesis.

Here, we read the statement as “there is no difference between our two sample means.” Equivalently, we interpret the statement as both sample means estimate the same population mean.

Under the Neyman-Pearson approach to inference we have two hypotheses: the null hypothesis and the alternative hypothesis. The hull hypothesis was defined above.

Alternative hypothesis

Alternative hypothesis (H_A): If we conclude that the null hypothesis is false, or rather and more precisely, we find that we provisionally fail to reject the null hypothesis, then we provisionally accept the alternative hypothesis. The view then is that something other than random chance has influenced the sample observations. Note that the pairing of null and alternative hypotheses covers all possible outcomes. We do not, however, say that we have evidence for the alternative hypothesis under this statistical regimen (Abelson 1995). We tested the null hypothesis, not the alternative hypothesis. Thus, it is incorrect to write that, having found a statistical difference between two drug treatments, say aspirin and acetaminophen for relief of migraine symptoms, it is not correct to conclude that we have proven the case that acetaminophen improves improves symptoms of migraine sufferers.

For the one sample, two tailed null hypothesis, the alternative hypothesis is

and we read it as “there is a statistical difference between our sample mean and the population mean.” For the two sample, two tailed null hypothesis, the alternative hypothesis would be

and we read it as “there is a statistical difference between our two sample means.”

Alternative hypothesis often may be the research hypothesis.

It may be helpful to distinguish between technical hypotheses, scientific hypothesis, or the equality of different kinds of treatments. Tests of technical hypotheses include the testing of statistical assumptions like normality assumption (see Chapter 13.3) and homogeneity of variances (Chapter 13.4). The results of inferences about technical hypotheses are used by the statistician to justify selection of parametric statistical tests (Chapter 13). The testing of some scientific hypothesis like whether or not there is a positive link between lifespan and insulin-like growth factor levels in humans (Fontana et al 2008), like the link between lifespan and IGFs in other organisms (Holtzenberger et al 2003), can be further advanced by considering multiple hypotheses and a test of nested hypotheses and evaluated either in Bayesian or likelihood approaches (Chapter 16 and Chapter 17). The advantage of the Bayesian approach is that it returns evidence for or against this hypothesis: if the posterior probability is greater than the prior probability, we can we say that we have evidence for the hypothesis. This is very appealing — the challenge is that the prior probability is inherently subjective (Chapter 6.4), limited by the amount and quality of existing information pertaining to the hypothesis (Prelec 2004).

How to interpret the results of a statistical test.

Any number of statistical tests may be used to calculate the value of the test statistic. For example, a one sample t-test may be used to evaluate the difference between the sample mean and the population mean (Chapter 8.5) or the independent sample t-test may be used to evaluate the difference between means of the control group and the treatment group (Chapter 10). The test statistic is the particular value of the outcome of our evaluation of the hypothesis and it is associated with the p-value. In other words, given the assumption of a particular probability distribution, in this case the t-distribution, we can associate a probability, the p-value, that we observed the particular value of the test statistic and the null hypothesis is true in the reference population.

By convention, we determine statistical significance (Cox 1982; Whitley & Ball 2002) by assigning ahead of time a decision probability called the Type I error rate, often given the symbol α (alpha). The practice is to look up the critical value that corresponds to the outcome of the test with degrees of freedom like your experiment and at the Type I error rate that you selected. The Degrees of Freedom (DF, df, or sometimes noted by the symbol v), are the number of independent pieces of information available to you. Knowing the degrees of freedom is a crucial piece of information for making the correct tests. Each statistical test has a specific formula for obtaining the independent information available for the statistical test. We first were introduced to DF when we calculated the sample variance with the Bessel correction, n – 1, instead of dividing through by n. With the df in hand, the value of the test statistic is compared to the critical value for our null hypothesis. If the test statistic is smaller than the critical value, we fail to reject the null hypothesis. If, however, the test statistic is greater than the critical value, then we provisionally reject the null hypothesis. This critical value comes from a probability distribution appropriate for the kind of sampling and properties of the measurement we are using. In other words, the rejection criterion for the null hypothesis is set to a critical value, which corresponds to a known probability, the Type I error rate.

Before proceeding with yet another interpretation, and hopefully less technical discussion about test statistics and critical values, we need to discuss the two types of statistical errors. The Type I error rate is the statistical error assigned to the probability that we may reject a null hypothesis as a result of our evaluation of our data when in fact in the reference population, the null hypothesis is, in fact, true. In Biology we generally use Type I error α = 0.05 level of significance. We say that the probability of obtaining the observed value AND H_O is true is 1 in 20 (5%) if α = 0.05. Put another way, we are willing to reject the Null Hypothesis when there is only a 5% chance that the observations could occur and the Null hypothesis is still true. Our test statistic is associated with the p-value; the critical value is associated with the Type I error rate. If and only if the test statistic value equals the critical value will the p-value equal the Type I error rate.

The second error type associated with hypothesis testing is, β, the Type II statistical error rate. This is the case where we accept or fail to reject a null hypothesis based on our data, but in the reference population, the situation is that indeed, the null hypothesis is actually false. We must also keep in mind that, as we evaluate the p-value relative to the magnitude of the Type I error rate, and if we reject the null hypothesis, we still do not say that we have evidence for the alternative hypothesis.

Thus, we end with a concept that may take you a while to come to terms with — there are four, not two possible outcomes of an experiment.

Outcomes of an experiment

What are the possible outcomes of a comparative experiment\? We have two treatments, one in which subjects are given a treatment and the other, subjects receive a placebo. Subjects are followed and an outcome is measured. We calculate the descriptive statistics aka summary statistics, means, standard deviations, and perhaps other statistics, and then ask whether there is a difference between the statistics for the groups. So, two possible outcomes of the experiment, correct\? If the treatment has no effect, then we would expect the two groups to have roughly the same values for means, etc., in other words, any difference between the groups is due to chance fluctuations in the measurements and not because of any systematic effect due to the treatment received. Conversely, then if there is a difference due to the treatment, we expect to see a large enough difference in the statistics so that we would notice the systematic effect due to the treatment.

Actually, there are four, not two, possible outcomes of an experiment, just as there were four and not two conclusions about the results of a clinical assay. The four possible outcomes of a test of a statistical null hypothesis are illustrated in Table 1.

Table 1. When conducting hypothesis testing, four outcomes are possible.

In the actual population, a thing happens or it doesn’t. The null hypothesis is either true or it is not. But we don’t have access to the reference population, we don’t have a census. In other words, there is truth, but we don’t have access to the truth. We can weight, assigned as a probability or p-value,  our decisions by how likely our results are given the assumption that the truth is indeed “no difference.”

If you recall, we’ve seen a table like Table 1 before in our discussion of conditional probability and risk analysis (Chapter 7.3). We made the point that statistical inference and the interpretation of clinical tests are similar (Browner and Newman 1987). From the perspective of ordering a diagnostic test, the proper null hypothesis would be the patient does not have the disease. For your review, here’s that table (Table 2).

Table 2. Interpretations of results of a diagnostic or clinical test.

Thus, a positive diagnostic test result is interpreted as rejecting the null hypothesis. If the person actually does not have the disease, then the positive diagnostic test is a false positive.

Questions

1. Match the corresponding entries in the two tables. For example, which outcome from the inference/hypothesis table matches specificity of the test \?
2. Find three sources on the web for definitions of the p-value. Write out these definitions in your notes and compare them.
3. In your own words distinguish between the test statistic and the critical value.
4. All of our discussions have been about testing the null hypothesis, about accepting or rejecting, provisionally, the null hypothesis.
5. What are the p-values for -logP of 5, 6, 7, 8, 9, and 10 \? Complete the p-value -logP transform table.
6. Instead of log₁₀ transform, create a similar table but for negative natural log transform. Which is more convenient? Hint: log(x, base=exp(1))

Quiz Chapter 8.1

The null and alternate hypothesis

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Chapter 8 contents

• Introduction
• The null and alternative hypotheses
• The controversy over proper hypothesis testing
• Sampling distribution and hypothesis testing
• Tails of a test
• One sample t-test
• Confidence limits for the estimate of population mean
• References and suggested readings

3.2 – Measures of Central Tendency

Introduction to summary statistics.

For a sample of observations we can begin the summary by identifying the “typical” value. Various statistics are used to describe the middle and collectively these are referred to as measures of central tendency. The mean, the median, and the mode are the most common measures of central tendency. In the situation in which we work with data from a population census, we would calculate population descriptive statistics — not inferential statistics; because we more often work with samples from populations, we report sample descriptive statistics.

First we review the familiar arithmetic mean and introduce the weighted mean. Next we introduce “other means,” which you may not be as familiar with.

Means.

There are several means beyond the simple arithmetic average or mean. Here we review a few. We use this topic also to start introducing standard notation we will use throughout the book.

The population mean, μ (pronounced “mu”) is given by

X_i, an observation on the i-th individual

Σ, or “sigma,” which instructs you to add them up (the X’s), from i = 1 (the first observation) to i = N (the last observation).

The sample mean, , pronounced “eks bar,” of a collection of observations is given by 

Weighted arithmetic mean.

In some cases you may have several samples from the same population. If the sample sizes are the same, you can calculate the average of averages without any fuss — just take all of the sample means and add them up, then divide by the total number of samples. If the sample sizes differ, then you needs to weight (W) each sample mean by its sample size. Simply divide each sample mean by its appropriate sample size, then add all of these up. That is the weighted average.

More generally, we can write

For example, consider a variable containing the following observations, for example, over the course of watching birds gathering at a drinking source (eg, recorded over 20 days, a single 5 minute interval per day), we can count how many times zero, one, two, etc birds are observed. 

Table 1. A sample of counts of observations, eg, how many birds

The observation “4” was observed four times; the observation “5” was observed twice, and so on for a total of 15 observations.

What is the arithmetic mean of these 15 observations? To solve this, well, you have a couple of choices. You could copy the numbers down as often as they appear and then calculate the mean in the usual way.

Other “means”.

The arithmetic average (illustrated above) is not the only way to estimate the mean.

The trimmed mean, also called the truncated mean, is a useful approach when data is widely dispersed — data spread away from the middle (see Chapter 3.3). Thus, the trimmed mean will be less influenced compared to the arithmetic mean by outlier data points, ie, data far from other data points in the set.

You would use the trimmed mean to describe the middle of a data set in which a plot shows most of the values are clumped together around a middle – and yet you see a few values that are much smaller or much greater. A specified percentage of the smallest and largest values are removed from the data set and then the simple arithmetic mean is calculated for the trimmed data set. For example, given a data set of daily rainfall for different cities, you might wish to remove the driest 5% and wettest 5% of the days in order to better compare the rainfall trends for the cities.

Calculating the trimmed mean is straight-forward in R: use the same built-in function, mean(), but add some options.

Note 2: This is a good time to remind you how to get help with R commands. Do you recall how to get help in R? 

At the R prompt type

help(mean) 

or

?mean

The R Documentation page for mean() will pop up (assuming you allowed R to install help pages as html). Figure 1 shows a screenshot of a portion of the help page for mean()

Figure 1. A portion of the R help page about the function mean.

From the help page (Fig 1) we can see that we can specify a trimmed mean by adding options to the mean(x, ...) command. For our x variable defined above, get the trimmed mean after 25% of the data are removed.

mean(x, trim=0.25)

[1] 6

From the help page we see that the only required option you need to feed the mean command is the name of the variable, in this case, “x” (it can be, of course, any name provided the data are attached). In this case we removed 25% of the values – 12.5% of the smallest values and 12.5% of the largest values – that’s also called the interquartile mean. We use a dot plot to show these trends (Fig 2).

Figure 2. Dot plot of our x variable with locations of the mean (blue) and the trimmed mean (red).  The Dotplot(x) function in package RcmdrMisc was used in Rcmdr to make this graphic. Arrows were added by hand. Dotplot() example code presented in Chapter 3.4.

If we recalculate a trimmed mean after dropping 10% of the points, or even 40% of the points, we get the same mean value of 6. The trimmed mean is an example of a robust estimator; it’s resistant to the influence of outliers.

Another useful descriptor of the middle is the geometric mean. The geometric mean is useful for calculating the average of ratios.  Geometric mean would be used when you want to compare central tendency for different variables, each differing in scale. For example, gene expression results, reported as fold-changes, for different genes often shows tremendous differences among genes and would be best described by logarithmic scale, not arithmetic scale. Geometric mean expression values would be better choice for central tendency. Other examples are found in economics: for example, calculating compound interest or interest. The geometric mean applies whenever the scale is multiplicative and not additive

The geometric mean is given by the equation

The geometric mean (gm) is equivalent to log-transforming your data, then calculating the arithmetic mean, and transforming the result back (with the antilog exponent.) As you recall, for our simple data set the arithmetic mean was 6.2. The geometric mean for this data was 5.977. Taking the natural log for each of the values from our simple data set, then calculating the arithmetic mean we have 1.788. 

The antilog of this value is

exp(1.788)

[1] 5.977

Another frequently encountered mean is the harmonic mean, which is defined by the equation

Harmonic mean is appropriate for averaging rates. For example, what is the average speed traveled if you travel 30 miles per hour (mph) between point A and B, then on the return trip, your speed was 40 mph? If you think (30 + 40)/2 = 35 mph, then this would be incorrect — after all, the distance covered has not changed, just the time. The harmonic mean returns 34.2 mph. Let

y = c(30,40)

The harmonic mean returns 34.2 mph ( see below “How to calculate these other means”)

Both harmonic and geometric means apply for values greater than zero.

How to calculate these “other” means.

In Microsoft Excel, calculate geometric mean via the function GEOMEAN(); calculate harmonic mean via the function HARMEAN().

The base R (and Rcmdr) doesn’t have built in functions for these, although you could download and install some R packages which do (eg, package psych, geometric.mean(variable), harmonic.mean(variable)). It is quicker to just to calculate these by submitting a snippet of code into the script window

For geometric mean of variable “x” at the R prompt type

exp(mean(log(x)))

For harmonic mean of variable “x” at the R prompt type

1/mean(1/x)

where is the base of the natural logarithm, Euler’s number, and log is the natural logarithm (in R, to get log to other bases you can use log10 for base 10 logarithm or log2 for base 2 logarithm, or  log(x, base = n) for any base n of the variable x, and variable is the name of the variable you wish to do the calculations on.

R code: Do try on your own!

Here’s some numbers to try your hand. For example, create a variable containing a few numbers, any numbers. and write it to the variable named z

myZ = c(3,4,6,7,9,11,4)

Now, calculate the arithmetic mean, the geometric mean, and the harmonic mean for the variable myZ. You should get Table 4.2)}

Table 2. Comparison of different means for myZ.

Try three more. In R (or R Commander script window), create three new variables.

varA = c(3,3,3,3)

varB = c(1,2,3,12)

varC = c(-3,0,1,3)

Now, calculate the arithmetic mean, geometric mean, and harmonic mean for each variable.

For the simple arithmetic mean

mean(varA)

For the geometric mean, use the formula above

exp(mean(log(varA)))

For the harmonic mean, use the formula above

1/mean(1/varA)

What did you get?

Other measures of central tendency

Median 

The median, which lacks an accepted notation — we’ll go with , divides a set of observed numbers into two equal halves. Half the observations are above the median, half of the observations are below the median. Arrange data from lowest to highest, take the middle measurement:

odd number of measurements minus the middle value minus even number of measurements minus average of the 2 middle values

Or, more succinctly, we have

To get the median in R type at the R prompt

median(variable)

and of course, replace variable with the name of the variable containing the numbers. For our x variable created earlier, the function median returns in R

[1] 6

[Note that the median for x was the same as the trimmed mean for x, which is consistent with with our view that the trimmed mean is a robust estimator of the middle of a data set.

Mode

Mode is another way to express the middle and it refers to the most frequent occurring measurement. Use of mode makes most sense for discrete or countable numbers. For a normal distribution, the mean, median and mode will be the same value. Note that a data set may have more than one mode. For example, what is the mode for the variable  we created earlier?

myX = c(4,4,4,4,5,5,6,6,6,7,7,8,8,8,15)

For this small data set we see that “4” is the most frequent with a count of four occurrences in the set.

Mode would seem like a straightforward function in R. However, it turns out there is not a mode function in the base package.

A little explanation is in order. In R, typing mode at the R prompt like so

mode(myX)

returns

[1] "numeric" 

Not the answer we were expecting. In R, mode command is used to tell you what the mode (ie, way or manner in which some task is accomplished) of storage is for the variables.

In order to get the statistical mode we want, we either hunt down a package that contains mode estimation (eg, install the package DescTools use the Mode function — see below), or we can write a little code.

A quick Google search found a number of answers at stackoverflow.com (eg, question 2547402). The simplest response was to use names and max commands like so

temp = table(as.vector(myX))

names (temp)[temp==max(temp)]

Why the median may be a better middle than the mean

Comparing the two measures of central tendency can tell you without plotting how your data are distributed about the middle. Sample distributions are discussed in Chapter 6. 

• When the distribution of the data is symmetric or normally distributed (discussed in Chapter 6.7) then the mean and the median will be about the same value
• When data are right-skewed (a few large values), then the mean will be greater than the median.
• When the data are left-skewed (a few small values), then the mean will be less than the median.

Here’s an illustration (Fig 3). I sampled 100 points from a random normal distribution with mean zero and standard deviation 0ne and another 100 points from a log-normal distribution also with mean zero and standard deviation one. In Figure 3, the histograms (see Chapter 4.2 – Histograms), along with summary statistics (see Note 4). Means are indicated with red arrows and medians are indicated with blue arrows.

Figure 3. Normal and lognormal distributions with mean (red) and median (blue) noted for comparison.

So the median is a better descriptor or the central tendency of a sample distribution when the distribution is NOT normally distributed.

Scaling and transformation of data

Sometimes it is useful to standardize your data so that the variables all have the same scale. One algorithm for standardization is called normalization. Normalization implies that you correct the data so that data has a mean, μ, of zero, and a standard deviation, σ, of 1 (unit variance). There are several ways to standardize, each with strengths and limitations. To normalize we use the Z-score equation (see Chapter 6.7 for other uses of Z score).

where X_i is each observation in your data set.

Normalization will make outliers, the few points in a data set that are noticeably different from the central tendency of the rest of the data, smaller and less influential. When you normalize multiple sets of data, then each will have the same mean (0) and variance (unit variance), but the ranges will differ. An example of this is the simple product moment correlation — by standardizing you change the variances for the different variables to have the same unit variance.

As we will see later in class it is also useful to expand or contract the variability of the data or to change the shape of the distribution (if the data is not normally distributed). For example, if you compare individuals of a population for many morphological traits (eg body size, growth rate), the spread of points (called a distribution) will look more like a Poisson distribution (not symmetrical about the mean, a few individuals may be much larger…). This is partly due to the way in which morphological traits are measured. We normally measure body size on a linear scale (inches or centimeters). However, body size is affected by physiological processes that are more related to volume. Therefore, the more appropriate scale of measurement is on a log scale. We can transform the data measured on a linear scale to a log scale. For morphological traits this can produce a distribution that is normally distributed (bell shape). There are many more statistical procedures for data that is normally distributed than there are statistical procedures for Poisson distributions or any other type of distribution. Additional discussion about data transformation is introduced in Chapter 13.3.

You can always uncode or unstandardize your data after performing the statistical procedures and return to the original scale. In fact, when reporting descriptive statistics you should report the untransformed, uncoded data. Moreover, you will find it useful to report means adjusted for other variables (eg, from ANOVA or regression); if the ANOVA or regression equations are performed on transformed or coded data you would want to back calculate to the original scale after applying the ANOVA or regression adjustments. This advise will make more sense after we’ve discussed ANOVA (Chapter 12) and linear regression (Chapter 17).

R operators

The names command can be used to retrieve the names contained in the variable (if text types) or to set the names of the observations, which is what we are using it for here. We set the numbers to text names “4”, “5”, etc. then find the maximum count of named items in the temp table. The double equals operator (==) is used to tell R to find the object that is “equal to” something we specify, in this case, the max value (R Language Definition 2014). Table 3 shows common operators in R.

Table 3. Common arithmetic* and comparison** operators

help(Arithmetic)

help(Comparison)

The R package modeest has a number of algorithms for calculating the mode, depending on the kind of data you are working with. After installing the package and its dependencies, type at the R prompt 

require(modeest)
mfv(myX)
[1] 4

Creating objects in R

Everything in R is an object (Chambers 2008). We provide many worked examples in Part 07. Working with your own data – Mike’s Workbook for Biostatistics. In brief, create a variable in R by assigning the vector x, either directly at the R prompt or in a script window (Rcmdr, RStudio), like so

myX = c(4,4,4,4,5,5,6,6,6,7,7,8,8,8,15)

The function c(), which stands for combine  is used to combine the set of numbers into the object, myX. For small sets like this you may find it convenient to enter the values one by one and let R store it into the vector for you. For R installed on your computer, use the scan() function and your keyboard — scan() doesn’t work consistently in serverless R instances (eg., Google CoLab). Careful! Make sure that you remember to assign the results from scan to a vector.

I’ll create the object tryScan just to distinguish it from x, although I will enter the same values. Until R receives an interrupt signal from you, it will prompt you to enter numbers one row at a time. When you’ve reached the end, use the keyboard shortcut Ctrl + q (Windows) or Cmd + q (macOS) to interrupt keyboard input. 

tryScan = scan()
1: 4
2: 4
3: 4
4: 4
5: 5
6: 5
7: 6
8: 6
9: 6
10: 7
11: 7
12: 8
13: 8
14: 8
15: 15
Read 15 items

tryScan
 [1] 4 4 4 4 5 5 6 6 6 7 7 8 8 8 15

The function tryScan is a very useful command, with many options, and can be used for more than keyboard entry. For example, you can paste from your computer’s clipboard a column of numbers from your spreadsheet.

R code calculate central tendency

Once we have the vectormyX, calculate the mean by entering at the R prompt

mean(myX)

and you should get the answer of 6.466667

And of course, you don’t type in the R prompt >, right?

Or, for the better option, create two variables, one containing the list of observed numbers and the second that contains the frequency for each observed number in the series. You would then use the command for weighted mean.

myY = c(4,5,6,7,8,15)

myW = c(4/15, 1/15, 3/15, 2/15, 4/15, 1/15)

Note — you can check that the frequencies sum to 1 by using the sum command like so

sum(myW)

For the weighted mean, the command is

weighted.mean(myY,myW)

and, the answer returned is 6.466667, the same as before.

There’s an R package for that.

We list code examples for all of the statistics described on this page, but as you can imagine, there are packages that include these and other useful functions, or “wrapper functions” that make writing code easier in R. A good example is the DescTools package. One advantage of using a package like DescTools is that it cuts through the need to remember specific commands for basic data exploration. For example, just call the Desc() function to yield several measures of central tendency and dispersion (see Chapter 3.3). 

The R code and output follows, along with a plot (Fig 4). The mean and median are highlighted in orange.

Desc(myX)
──────────────────────────────────────────────────────────────────────────────── 
myX (numeric)

length      n   NAs unique   0s  mean meanCI'
    15     15     0      6    0  6.47    4.92
       100.0%  0.0%        0.0%          8.02

   .05    .10   .25 median  .75   .90     .95
  4.00   4.00  4.50   6.00 7.50  8.00   10.10

range      sd vcoef    mad  IQR  skew    kurt
11.00    2.80  0.43   2.97 3.00  1.72    2.94

  value freq   perc cumfreq cumperc
1     4    4  26.7%       4   26.7%
2     5    2  13.3%       6   40.0%
3     6    3  20.0%       9   60.0%
4     7    2  13.3%      11   73.3%
5     8    3  20.0%      14   93.3%
6    15    1   6.7%      15  100.0%

' 95%-CI (classic)

Figure 4. Histogram, box plot, and cumulative distribution function plot generated by default by Desc() call.

Lots of output! This is a good example of how to explore data — describe the middle (eg, mean and median), but also the variability about the middle (eg, range, standard deviation — sd, mean absolute deviation — mad, coefficient of variation — vcoef), and distribution shape (quantiles — 0.05, 0.25 etc, kurt, skew). The plots — histogram, box plot, and cumulative distribution plots — are explained in Chapter 4.

Use aggregate() to calculate summary statistics by group.

So far, all code presumes need to calculate descriptive statistics one vector at a time. In general, we need summary statistics for more than one group or strata. For example, we may ask, what are the average body temperature readings measured by IR device on different body areas from several subjects (question 8a, Homework 2A: Descriptive statistics in Mike’s Workbook for Biostatistics).

The aggregate() function in R simplifies calculating means by groups by providing a concise and efficient way to apply a summary function (like mean()) to a variable, grouped by one or more other variables. The format for aggregate is

 aggregate(x = variable_to_aggregate ~ grouping_variable, FUN = mean, data = your_dataframe)

Questio8a had two levels of body regions, “Forehead” and “Throat.” Assuming the variable is named bodyTemp and the grouping variable is called bodyGroup and stored in the attached data.frame question08a, then the following R code provides the requested summary statistics by groups.

aggregate(bodyTemp ~ bodyGroup, data = question08a, 
function(x) c(mean = mean(x)))

Additional statistics can be requested by adding one after the other following mean(x), eg, median = median(x).

The advantage of use of R Commander, it’s easy to get multiple statistics by groups by following the drop down menus, beginning with Statistics > Summaries > Table of statistics… (Fig 5).

Figure 5. Screenshot R Commander, summary statistics by group.

Questions

1. Find the help page in R for the median function. How does the function handle missing values?
2. For a simple data set like the following myY <- c(1,1,3,6) you should now be able to calculate, by hand, the
   • mean • median • mode
3. If the observations for a ratio scale variable are normally (symmetrically) distributed, which statistic of central tendency is best (eg, less sensitive to outlier values)?
4. In the names() command, what do you think the result will be if you replace max in the command with min?
5. If data are right skewed, what will be the order of the mean, median, and mode?
6. Body mass of Rhinella marina (formerly Bufo marinus, Fig 6),
   bufo <- c(71.3, 71.4, 74.1, 85.4, 85.4, 86.6, 97.4, 99.6, 107, 115.7, 135.7, 156.2)

Figure 6. Female Rhinella marina (formerly Bufo marinus), Chaminade University campus. Body length 23.5 cm. Click image to view full sized image.

7. Under what circumstances is it appropriate to transform raw data?
8. What does “standardize” or “normalize” imply as actions to take with data?

Quiz Chapter 3.2

Measures of Central Tendency

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Chapter 3 contents

• Exploring data
• Data types
• Measures of Central Tendency
• Measures of dispersion
• Estimating parameters
• Statistics of error
• References and suggested readings