My coursework from BIMM 143. Showcasing genomic analysis techniques, introductory machine learning, and protein folding and structure prediction.
Aadhya Tripathi (PID: A17878439)
There are lots of ways to make plots in R. These include so-called “base
R” (like the plot()) and add-on packages like ggplot2.
Let’s make the same plot with these two graphics systems. We can use the
inbuilt cars dataset:
head(cars)
speed dist
1 4 2
2 4 10
3 7 4
4 7 22
5 8 16
6 9 10
With “base R” we can simply:
plot(cars)

Now let’s try ggplot. First, I need to install the package using
install.packages("ggplot2").
N.B. We never run an
install.packages()in a code chunk, otherwise we will needlessly re-install every time we render the document.
Every time we want to use an add-on, we need to load it up with a call
to library()
library(ggplot2)
ggplot(cars)

Every ggplot needs AT LEAST 3 things:
ggplot(cars) +
aes(x=speed, y=dist) +
geom_point() +
geom_smooth(method = "lm", se = FALSE) +
labs(x="Speed (MPH)",
y="Distance (ft)",
title="Stopping Distance of Old Cars") +
theme_bw()
`geom_smooth()` using formula = 'y ~ x'

Read some data on the effects of GLP-1 inhibitor drug on gene expression values.
url <- "https://bioboot.github.io/bimm143_S20/class-material/up_down_expression.txt"
genes <- read.delim(url)
head(genes)
Gene Condition1 Condition2 State
1 A4GNT -3.6808610 -3.4401355 unchanging
2 AAAS 4.5479580 4.3864126 unchanging
3 AASDH 3.7190695 3.4787276 unchanging
4 AATF 5.0784720 5.0151916 unchanging
5 AATK 0.4711421 0.5598642 unchanging
6 AB015752.4 -3.6808610 -3.5921390 unchanging
Version 1 plot - starting simple
ggplot(genes) +
aes(Condition1, Condition2) +
geom_point(col="blue", alpha=0.3)

Let’s color by the State - up, down, or not changing. table() counts
occurences of a value in a vector.
table(genes$State)
down unchanging up
72 4997 127
ggplot(genes) +
aes(x=Condition1, y=Condition2, col=State) +
geom_point() +
scale_color_manual(values = c("purple","gray","red")) +
labs(x="Control (no drug)",
y="GLP-1 Drug Treatment",
title="Changes in Gene Expression in Response to GLP-1 Drug") +
theme_light()

Explore the famous gapminder dataset with custom plots.
# File location online
url <- "https://raw.githubusercontent.com/jennybc/gapminder/master/inst/extdata/gapminder.tsv"
gapminder <- read.delim(url)
head(gapminder)
country continent year lifeExp pop gdpPercap
1 Afghanistan Asia 1952 28.801 8425333 779.4453
2 Afghanistan Asia 1957 30.332 9240934 820.8530
3 Afghanistan Asia 1962 31.997 10267083 853.1007
4 Afghanistan Asia 1967 34.020 11537966 836.1971
5 Afghanistan Asia 1972 36.088 13079460 739.9811
6 Afghanistan Asia 1977 38.438 14880372 786.1134
Q. How many rows does the gapminder dataset have?
nrow(gapminder)
[1] 1704
Q. How many different continents are in this dataset?
table(gapminder$continent)
Africa Americas Asia Europe Oceania
624 300 396 360 24
Version 1, plot gdpPercap vs LifeExp for all rows
ggplot(gapminder) +
aes(gdpPercap, lifeExp, col=continent) +
geom_point()

Construct a plot for each continent, separately. Inn ggplot, this is called “faceting”.
ggplot(gapminder) +
aes(gdpPercap, lifeExp, col=continent) +
geom_point() +
facet_wrap(~continent)

Another add-on package with a function called filter() that we want to
use.
library(dplyr)
Attaching package: 'dplyr'
The following objects are masked from 'package:stats':
filter, lag
The following objects are masked from 'package:base':
intersect, setdiff, setequal, union
filter(gapminder, year==2007, country=="India")
country continent year lifeExp pop gdpPercap
1 India Asia 2007 64.698 1110396331 2452.21
input <- filter(gapminder, year==2007 | year==1977)
ggplot(input) +
aes(gdpPercap, lifeExp, col=continent) +
geom_point() +
facet_wrap(~year)
