Original post

One morning, while seeing a mention of a disease on Hacker News, Bob decides on
a whim to get tested for it; there are no other symptoms, he’s just curious. He
convinces his doctor to order a blood test, which is known to be 90% accurate.
For 9 out of 10 sick people it will detect the disease (but for 1 out of 10 it
won’t); similarly, for 9 out of 10 healthy people it will report no disease (but
for 1 out of 10 it will).

Unfortunatly for Bob, his test is positive; what’s the probability that Bob
actually has the disease?

You might be tempted to say 90%, but this is wrong. One of the most common
fallacies made in probability and statistics is mixing up conditional
probabilities. Given event D – “Bob has disease” and event T – “test was
positive”, we want to know what is P(D|T) – the conditional probability
of D given T. But the test result is actually giving us P(T|D) – which
is distinct from P(D|T).

In fact, the problem doesn’t provide enough details to answer the question. An
important detail that’s missing is the prevalence of the disease in
population; that is, the value of P(D) without being conditioned on
anything. Let’s say that it’s a moderately common disease with 2% prevalence.

To solve this without any clever probability formulae, we can resort to the
basic technique of counting by cases. Let’s assume there is a sample of 10,000
people ; test aside, how many of them have the disease? 2%, so 200. Of the people who have the disease, 90% will test positive and 10% will test
negative. Similarly, of the people with no disease, 90% will test negative and
10% will test positive. Graphically: Now we just have to count. There are 980 + 180 = 1160 people who tested positive
in the sample population. Of these people, 180 have the disease. In other words,
given that Bob is in the “tested positive” population, his chance of having
the disease is 180/1160 = 15.5%. This is far lower than the 90% test accuracy;
conditional probability often produces surprising results. To motivate this,
consider that the number of true positives (people with the disease that
tested positive) is 180, while the number of false positives (people w/o the
disease that tested positive) is 980. So the chance of being in the second group
is larger.

## Conditional probability

As the examples shown above demonstrate, conditional probabilities involve
questions like “what’s the chance of A happening, given that B happened”, and
they are far from being intuitive. Luckily, the mathematical theory of
probability gives us the precise and rigorous tools necessary to reason about
such problems with relative elegance.

The conditional probability P(A|B) means “what is the probability of
event A given that we know event B occurred”. Its mathematical definition is:

[P(A|B)=frac{P(Acap B)}{P(B)}]

Notes:

• Obviously, this is only defined when P(B)>0.
• Here P(Acap B) is the probability that both A and B occurred.

The first time you look at it, the definition of conditional probability looks
somewhat unintuitive. Why is the connection made this way? Here’s a
visualization that I found useful: The dots in the black square represent the “universe”, our whole sampling
space (let’s call it S, and then P(S)=1). A and B are events. Here
P(A)=frac{30}{64} and P(B)=frac{18}{64}. But what is
P(A|B)? Let’s figure it out graphically. We know that the outcome is one
of the dots encircled in red. What is the chance we got a dot also encircled in
blue? It’s the number of dots that are both red and blue, divided by the total
number of dots in red. Probabilities are calculated as these counts normalized
by the size of the whole sample space; all the numbers are divided by 64, so
these denominators cancel out; we’ll have:

[P(A|B)=frac{P(Acap B)}{P(B)} = frac{9}{18} = frac{1}{2}]

In words – the probability that A happened, given that B happened, is 1/2, which
makes sense when you eyeball the diagram, and assuming events are uniformly
distributed (that is, no dot is inherently more likely to be the outcome than
any other dot).

Another explanation that always made sense to me was to multiply both sides of
the definition of conditional probability by the denominator, to get:

[P(A|B)P(B)=P(Acap B)]

In words: we know the chance that A happens given B; if we multiply this by the
chance that B happens, we get the chance both A and B happened.

Finally, since P(Acap B)=P(Bcap A), we can freely exchange A and B in
these definitions (they’re arbitrary labels, after all), to get:

[begin{equation}
P(Acap B)=P(A|B)P(B)=P(B|A)P(A) tag{1}
end{equation}]

This is an important equation we’ll use later on.

## Independence of events

By definition, two events A and B are independent if:

[P(Acap B)=P(A)P(B)]

Using conditional probability, we can provide a slightly different definition.
Since:

[P(A|B)=frac{P(Acap B)}{P(B)}]

And P(Acap B)=P(A)P(B):

[P(A|B)=frac{P(A)P(B)}{P(B)}=P(A)]

As long as P(B)>0, for independent A and B we have
P(A|B)=P(A); in words – B doesn’t affect the probability of A in any
way. Similarly we can show that for P(A)>0 we have P(B|A)=P(B).

Independence also extends to the complements of events. Recall that
P(B^C) is the probability that B did not occur, or 1-P(B);
since conditional probabilities obey the usual probability axioms, we
have: P(B^C|A)=1-P(B|A). Then, if A and B are independent:

[P(B^C|A)=1-P(B)=P(B^C)]

Therefore, B^C is independent of A. Similarly the complement of A is
independent of B, and the two complements are independent of each other.

## Bayes’ theorem

Starting with equation (1) from above:

[P(Acap B)=P(A|B)P(B)=P(B|A)P(A)]

And taking the right-hand-side equality and dividing it by P(B) (which
is positive, per definition), we get Bayes’s theorem:

[P(A|B)=frac{P(B|A)P(A)}{P(B)}]

This is an extremely useful result, because it links P(B|A) with
P(A|B). Recall the disease test example, where we’re looking for
P(D|T). We can use Bayes theorem:

[P(D|T)=frac{P(T|D)P(D)}{P(T)}]

We know P(T|D) and P(D), but what is P(T)? You may be
tempted to say it’s 1 because “well, we know the test is positive” but that
would be a mistake. To understand why, we have to dig a bit deeper into the
meanings of conditional vs. unconditional probabilities.

## Prior and posterior probabilities

Fundamentally, conditional probability helps us address the following question:

How do we update our beliefs in light of new data?

Prior probability is our beliefs (probabilities assigned to events) before we
see the new data. Posterior probability is our beliefs after we see the new
data. In the Bayes equation, prior probabilities are simply the un-conditioned
ones, while posterior probabilities are conditional. This leads to a key
distinction:

• P(T|D): posterior probability of the test being positive when we have
new data about the person – they have the disease.
• P(T): prior probability of the test being positive before we know

This should make it clearer why we can’t just assign P(T)=1. Instead,
recall the “counting by cases” exercise we did in the first example, where we
produced a tree of all possibilities; let’s formalize it.

## Law of Total Probability

Suppose we have the sample space S and some event B. Sometimes it’s easier to
find the probability of B by first partitioning the space into disjoint pieces: Then, because the probabilities of A_n are disjoint, we get:

[P(B)=P(Bcap A_1)+P(Bcap A_2)+P(Bcap A_3)+P(Bcap A_4)]

Or, using equation (1):

[P(B)=P(B|A_1)P(A_1)+P(B|A_2)P(A_2)+P(B|A_3)P(A_3)+P(B|A_4)P(A_4)]

## Bayesian solution to the disease test example

Now we have everything we need to provide a Bayesian solution to the disease
test example. Recall that we already know:

• P(T|D)=0.9: test accuracy
• P(D)=0.02: disease prevalance in the population

Now we want to compute P(T). We’ll use the law of total probability,
with the space partitioning of “has disease” / “does not have disease”:

[P(T)=P(T|D)P(D)+P(T|D^C)P(D^C)=0.9ast 0.02+0.1ast 0.98=0.116]

Finally, plugging everything into Bayes theorem:

[P(D|T)=frac{P(T|D)P(D)}{P(T)}

begin{align*}
P(D|T)&=frac{P(T|D)P(D)}{P(T)}
&=frac{P(T|D)P(D)}{0.116}
&=frac{0.9ast 0.02}{0.116}=0.155
end{align*}]

Which is the same result we got while working through possibilities in the
example.

## Conditioning on multiple events

We’ve just computed P(D|T) – the conditional probability of event D
(patient has disease) on event T (patient tested positive). An important
extension of this technique is being able to reason about multiple tests, and
how they affect the conditional probability. We’ll want to compute
P(D|T_1cap T_2) where T_1 and T_2 are two events for
different tests.

Let’s assume T_1 is our original test. T_2 is a slightly
different test that’s only 80% accurate. Importantly, the tests are
independent (they test completely different things) .

We’ll start with a naive approach that seems reasonable. For T_1, we
already know that P(D|T_1)=0.155. For T_2, it’s similarly simple
to compute:

[P(D|T_2)=frac{P(T_2|D)P(D)}{P(T_2)}]

The disease prevalence is still 2%, and using the law of total probability we
get:

[P(T_2)=P(T_2|D)P(D)+P(T_2|D^C)P(D^C)=0.8ast 0.02+0.2ast 0.98=0.212]

Therefore:

[P(D|T_2)=frac{P(T_2|D)P(D)}{P(T_2)}=frac{0.8ast 0.02}{0.212}=0.075]

In other words, if a person tests positive with the second test, the chance of
being sick is only 7.5%. But what if they tested positive for both tests?

Well, since the tests are independent we can do the usual probability trick of
combining the complements. We’ll compute the probability the person is not
sick given positive tests, and then compute the complement of that.
P(D^C|T_1)=1-0.155=0.845, and P(D^C|T_2)=1-0.075=0.925.
Therefore:

[P(D^C|T_1cap T_2)=P(D^C|T_1)P(D^C|T_2)=0.845ast 0.925=0.782]

And complementing again, we get P(D|T_1cap T_2)=1-0.782=0.218. The
chance of being sick, having tested positive both times is 21.8%.

Unfortunately, this computation is wrong, very wrong. Can you spot why before

We’ve committed a fairly common blunder in conditional probabilities. Given the
independence of P(T_1|D) and P(T_2|D), we’ve assumed the
independence of P(D|T_1) and P(D|T_2), but this is wrong! It’s
even easy to see why, given our concrete example. Both of them have P(D)
– the disease prevalence – in the numerator. Changing the prevalence will change
both P(D|T_1) and P(D|T_2) in exactly the same proportion; say,
increasing the prevalence 2x will increase both probabilities 2x. They’re
pretty strongly dependent!

The right way of finding P(D|T_1cap T_2) is working from first
principles. T_1cap T_2 is just another event, so treating it as such
and using Bayes theorem we get:

[P(D|T_1cap T_2)=frac{P(T_1cap T_2|D)P(D)}{P(T_1cap T_2)}]

Here P(D) is still 0.02; P(T_1cap T_2|D)=0.9ast0.8=0.72. To
compute the denominator we’ll use the law of total probability again:

[P(T_1cap T_2)=P(T_1cap T_2|D)P(D)+P(T_1cap T_2|D^C)P(D^C)=0.72ast 0.02+0.1ast 0.2ast 0.98=0.034]

Combining them all together we’ll get P(D|T_1cap T_2)=0.42; the chance
of being sick, given two positive tests, is 42%, which is twice higher than our
erroneous estimate .

## Bayes theorem with conditioning

Since conditional probabilities satistfy all probability axioms, many theorems
remain true when adding a condition. Here’s Bayes theorem with extra
conditioning on event C:

[P(A|Bcap C)=frac{P(B|Acap C)P(A|C)}{P(B|C)}]

In other words, the connection between P(A|B) and P(B|A) is true
even when everything is conditioned on some event C. To prove it, we can take
both sides and expand the definitions of conditional probability until we reach
something trivially true:

[begin{align*}
P(A|Bcap C)&=frac{P(B|Acap C)P(A|C)}{P(B|C)}
frac{P(Acap Bcap C)}{P(Bcap C)}&=frac{P(Acap Bcap C)P(A|C)}{P(Acap C)P(B|C)}
frac{P(Acap Bcap C)}{P(Bcap C)}&=frac{P(Acap Bcap C)P(Acap C)}{P(Acap C)P(B|C)P(C)}
end{align*}]

Assuming that P(Acap C)>0, it cancels out (similarly for P(C)>0
in a later step):

[begin{align*}
frac{P(Acap Bcap C)}{P(Bcap C)}&=frac{P(Acap Bcap C)}{P(B|C)P(C)}
frac{P(Acap Bcap C)}{P(Bcap C)}&=frac{P(Acap Bcap C)P(C)}{P(Bcap C)P(C)}
frac{P(Acap Bcap C)}{P(Bcap C)}&=frac{P(Acap Bcap C)}{P(Bcap C)}
end{align*}]

Q.E.D.

Using this new result, we can compute our two-test disease exercise in another
way. Let’s say that T_1 happens first, and we’ve already computed
P(D|T_1). We can now treat this as the new prior data, and find
P(D|T_1cap T_2) based on the new evidence that T_2 happened.
We’ll use the conditioned Bayes formulation with T_1 being C.

[P(D|T_2cap T_1)=frac{P(T_2|Dcap T_1)P(D|T_1)}{P(T_2|T_1)}]

P(T_2|Dcap T_1)? Since the tests are independent,
this is actually equivalent to P(T_2|D), which is 0.8. The denominator
requires a bit more careful computation:

[P(T_2|T_1)=frac{P(T_1cap T_2)}{P(T_1)}]

We’ve already found P(T_1)=0.116 previously, using the law of total
probability. Using the same law:

[P(T_1cap T_2)=P(T_1cap T_2|D)P(D)+P(T_2cap T_2|D^C)P(D^C)=0.9ast 0.9ast 0.02+0.1ast 0.2ast 0.98=0.034]

Therefore, P(T_2|T_1)=frac{0.034}{0.116}=0.293 and we now have all the
ingredients:

[P(D|T_2cap T_1)=frac{0.8ast 0.155}{0.293}=0.42]

We’ve reached the same result using two different approaches, which is
reassuring. Computing with both tests taken together is a bit quicker, but
taking one test at a time is also useful because it lets us update our beliefs
over time, given new data.

Computing conditional probabilities w.r.t. multiple parameters is very useful
in machine learning – this would be a good topic for a separate article.

  This actual number of people is arbitrary, and it could be anything else; in formulae it cancels out anyway. I picked 10,000 because it’s a nice number ending with a bunch of zeros and won’t produce fractional people for this particular example.
  You may be suspicious of this assumption – how can two tests for the same disease be independent? Being suspicious about probability independence assumptions is a good idea in general, but here the assumption is reasonable. Note that we assume independence given D; in other words, that P(T_1|D) and P(T_2|D) are independent. We know the person is sick, and we know that T_1 turned positive – does this affect T_2? Depends on the test; some tests definitely test related things, but some may test unrelated things (say the first looks for a particular by-product of sick cells while the second looks for a gene that is known to be correlated with disease prevalence). It’s possible to find plausible connections between almost anything though, so all independence assumptions are “best-effort”.
  My intuition for understanding why it’s higher is that there’s a tug of war between the test accuracy and the prevalence (the lower the prevalence, the higher the test accuracy has to be to produce reasonable predivtive value). But when we recompute with two tests, we still use prevalence just once in the formula, so the two tests combine forces against it.