Random Programs
Cash
In cash.py
we will calculate the minimum number of coins required to give a user change.
Ex:
$ python cash.py
Change owed: 0.41
4
We will first ask a user how much changed they are owed and then tell them the minimum number of coins (.25, .10, .05, and .01) with which said change can be made.
We will utilized get_float
from the CS50 library to get the user's input and print()
to output the answer.
Remember, if the user provides a non-negative value, our program should reprompt the user for a valid amount again and again until the user complies.
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Readability
In readability.py
we will compute the approximate grade level of given text.
Ex:
$ python readability.py
Text: Congratulations! Today is your day. You're off to Great Places! You're off and away!
Grade 3
readbility.c
, which uses the Coleman-Liau index to output grade level from text, but created using Python. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 |
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DNA
In this dna.py
we will identify a person based on their DNA.
DNA, the carrier of genetic information in living things, has been used in criminal justice for decades. But how, exactly, does DNA profiling work? Given a sequence of DNA, how can forensic investigators identify to whom it belongs?
Well, DNA is really just a sequence of molecules called nucleotides, arranged into a particular shape (a double helix). Each nucleotide of DNA contains one of four different bases: adenine (A), cytosine (C), guanine (G), or thymine (T). Every human cell has billions of these nucleotides arranged in sequence. Some portions of this sequence (i.e. genome) are the same, or at least very similar, across almost all humans, but other portions of the sequence have a higher genetic diversity and thus vary more across the population.
One place where DNA tends to have high genetic diversity is in Short Tandem Repeats (STRs). An STR is a short sequence of DNA bases that tends to repeat consecutively numerous times at specific locations inside of a person’s DNA. The number of times any particular STR repeats varies a lot among individuals. In the DNA samples below, for example, Alice has the STR AGAT
repeated four times in her DNA, while Bob has the same STR repeated five times.
Alice: | CT | AGAT | AGAT | AGAT | AGAT | GACT | A | |
Bob: | CT | AGAT | AGAT | AGAT | AGAT | AGAT | T |
Using multiple STRs, rather than just one, can improve the accuracy of DNA profiling. If the probability that two people have the same number of repeats for a single STR is 5%, and the analyst looks at 10 different STRs, then the probability that two DNA samples match purely by chance is about 1 in 1 quadrillion (assuming all STRs are independent of each other). So if two DNA samples match in the number of repeats for each of the STRs, the analyst can be pretty confident they came from the same person. CODIS, The FBI’s DNA database, uses 20 different STRs as part of its DNA profiling process.
What might such a DNA database look like? Well, in its simplest form, you could imagine formatting a DNA database as a CSV file, wherein each row corresponds to an individual, and each column corresponds to a particular STR.
name,AGAT,AATG,TATC
Alice,28,42,14
Bob,17,22,19
Charlie,36,18,25
AGAT
repeated 28 times consecutively somewhere in her DNA, the sequence AATG
repeated 42 times, and TATC
repeated 14 times. Bob, meanwhile, has those same three STRs repeated 17 times, 22 times, and 19 times, respectively. And Charlie has those same three STRs repeated 36, 18, and 25 times, respectively. So given a sequence of DNA, how might you identify to whom it belongs? Well, imagine that you looked through the DNA sequence for the longest consecutive sequence of repeated AGAT
s and found that the longest sequence was 17 repeats long. If you then found that the longest sequence of AATG
is 22 repeats long, and the longest sequence of TATC
is 19 repeats long, that would provide pretty good evidence that the DNA was Bob’s. Of course, it’s also possible that once you take the counts for each of the STRs, it doesn’t match anyone in your DNA database, in which case you have no match.
In practice, since analysts know on which chromosome and at which location in the DNA an STR will be found, they can localize their search to just a narrow section of DNA. But we’ll ignore that detail for this problem.
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