Learning Objectives
We are going to use part of the data published by Blackmore et al. (2017), The effect of upper-respiratory infection on transcriptomic changes in the CNS. The goal of the study was to determine the effect of an upper-respiratory infection on changes in RNA transcription occuring in the cerebellum and spinal cord post infection. Gender matched eight week old C57BL/6 mice were inoculated saline or with Influenza A by intranasal route and transcriptomic changes in the cerebellum and spinal cord tissues were evaluated by RNA-seq at days 0 (non-infected), 4 and 8.
The dataset is stored as a comma separated value (CSV) file. Each row holds information for a single RNA expression measurement, and the columns represent:
Column | Description |
---|---|
gene | The name of the gene that was measured |
sample | The name of the sample the gene expression was measured in |
expression | The value of the gene expression |
organism | The organism/species - here all data stem from mice |
age | The age of the mouse (all mice were 8 weeks here) |
sex | The sex of the mouse |
infection | The infection state of the mouse, i.e. infected with Influenza A or not infected. |
strain | The Influenza A strain; C57BL/6 in all cases. |
time | The duration of the infection (in days). |
tissue | The tissue that was used for the gene expression experiment, i.e. cerebellum or spinal cord. |
mouse | The mouse unique identifier. |
ENTREZID | The gene ID for the ENTREZ database |
product | The gene product |
ensembl_gene_id | The ID of the gene from the ENSEMBL database |
external_synonym | A name synonym for the gene |
chromosome_name | The chromosome name of the gene |
gene_biotype | The gene biotype |
phenotype_description | The phenotype description of the gene |
hsapiens_homolog_associated_gene_name | The human homologous gene |
We are going to use the R function download.file()
to download the
CSV file that contains the gene expression data, and we will use
read.csv()
to load into memory the content of the CSV file as an
object of class data.frame
. Inside the download.file()
function,
the first entry is a character string with the source URL. This source
URL downloads a CSV file from a GitHub repository. The text after the
comma ("data/rnaseq.csv"
) is the destination of the file on your
local machine. You’ll need to have a folder on your machine called
"data"
where you’ll download the file. So this command downloads the
remote file, names it "rnaseq.csv"
and adds it to a preexisting
folder named "data"
.
download.file(url = "https://raw.githubusercontent.com/UCLouvain-CBIO/WSBIM1207/master/data/rnaseq.csv",
destfile = "data/rnaseq.csv")
Alternatively, you can download the file manually and move it in the data directory in your RStudio project. This approach however has the drawback of loosing the provenance of the data.
You are now ready to load the data:
This statement doesn’t produce any output because, as you might recall, assignments don’t display anything. If we want to check that our data has been loaded, we can see the contents of the data frame by typing its name:
Wow… that was a lot of output. At least it means the data loaded
properly. Let’s check the top (the first 6 lines) of this data frame
using the function head()
:
## gene sample expression organism age sex infection strain
## 1 Asl GSM2545336 1170 Mus musculus 8 Female InfluenzaA C57BL/6
## 2 Apod GSM2545336 36194 Mus musculus 8 Female InfluenzaA C57BL/6
## 3 Cyp2d22 GSM2545336 4060 Mus musculus 8 Female InfluenzaA C57BL/6
## 4 Klk6 GSM2545336 287 Mus musculus 8 Female InfluenzaA C57BL/6
## 5 Fcrls GSM2545336 85 Mus musculus 8 Female InfluenzaA C57BL/6
## time tissue mouse ENTREZID
## 1 8 Cerebellum 14 109900
## 2 8 Cerebellum 14 11815
## 3 8 Cerebellum 14 56448
## 4 8 Cerebellum 14 19144
## 5 8 Cerebellum 14 80891
## product
## 1 argininosuccinate lyase, transcript variant X1
## 2 apolipoprotein D, transcript variant 3
## 3 cytochrome P450, family 2, subfamily d, polypeptide 22, transcript variant 2
## 4 kallikrein related-peptidase 6, transcript variant 2
## 5 Fc receptor-like S, scavenger receptor, transcript variant X1
## ensembl_gene_id external_synonym chromosome_name gene_biotype
## 1 ENSMUSG00000025533 2510006M18Rik 5 protein_coding
## 2 ENSMUSG00000022548 <NA> 16 protein_coding
## 3 ENSMUSG00000061740 2D22 15 protein_coding
## 4 ENSMUSG00000050063 Bssp 7 protein_coding
## 5 ENSMUSG00000015852 2810439C17Rik 3 protein_coding
## phenotype_description
## 1 abnormal circulating amino acid level
## 2 abnormal lipid homeostasis
## 3 abnormal skin morphology
## 4 abnormal cytokine level
## 5 decreased CD8-positive alpha-beta T cell number
## hsapiens_homolog_associated_gene_name
## 1 ASL
## 2 APOD
## 3 CYP2D6
## 4 KLK6
## 5 FCRL2
## [ reached 'max' / getOption("max.print") -- omitted 1 rows ]
Note
read.csv()
assumes that fields are delineated by commas, however, in
several countries, the comma is used as a decimal separator and the
semicolon (;) is used as a field delineator. If you want to read in
this type of files in R, you can use the read.csv2()
function. It
behaves exactly like read.csv()
but uses different parameters for
the decimal and the field separators. If you are working with another
format, they can be both specified by the user. Check out the help for
read.csv()
by typing ?read.csv
to learn more. There is also the
read.delim()
for in tab separated data files. It is important to
note that all of these functions are actually wrapper functions for
the main read.table()
function with different arguments. As such,
the data above could have also been loaded by using read.table()
with the separation argument as ,
. The code is as follows:
The header argument has to be set to TRUE
to be able to read the
headers as by default read.table()
has the header argument set to
FALSE. The quote argument has to be set to "\""
to only allow ” as a
quoting character (see how the product
variable for gene Rtca
in
rnaseq.csv
is written).
Data frames are the de facto data structure for most tabular data, and what we use for statistics and plotting.
A data frame can be created by hand, but most commonly they are
generated by the functions read.csv()
or read.table()
; in other
words, when importing spreadsheets from your hard drive (or the web).
A data frame is the representation of data in the format of a table where the columns are vectors that all have the same length. Because columns are vectors, each column must contain a single type of data (e.g., characters, integers, factors). For example, here is a figure depicting a data frame comprising a numeric, a character, and a logical vector.
We can see this when inspecting the structure of a data frame
with the function str()
:
## 'data.frame': 32428 obs. of 19 variables:
## $ gene : chr "Asl" "Apod" "Cyp2d22" "Klk6" ...
## $ sample : chr "GSM2545336" "GSM2545336" "GSM2545336" "GSM2545336" ...
## $ expression : int 1170 36194 4060 287 85 782 1619 288 43217 1071 ...
## $ organism : chr "Mus musculus" "Mus musculus" "Mus musculus" "Mus musculus" ...
## $ age : int 8 8 8 8 8 8 8 8 8 8 ...
## $ sex : chr "Female" "Female" "Female" "Female" ...
## $ infection : chr "InfluenzaA" "InfluenzaA" "InfluenzaA" "InfluenzaA" ...
## $ strain : chr "C57BL/6" "C57BL/6" "C57BL/6" "C57BL/6" ...
## $ time : int 8 8 8 8 8 8 8 8 8 8 ...
## $ tissue : chr "Cerebellum" "Cerebellum" "Cerebellum" "Cerebellum" ...
## $ mouse : int 14 14 14 14 14 14 14 14 14 14 ...
## $ ENTREZID : int 109900 11815 56448 19144 80891 20528 97827 118454 18823 14696 ...
## $ product : chr "argininosuccinate lyase, transcript variant X1" "apolipoprotein D, transcript variant 3" "cytochrome P450, family 2, subfamily d, polypeptide 22, transcript variant 2" "kallikrein related-peptidase 6, transcript variant 2" ...
## $ ensembl_gene_id : chr "ENSMUSG00000025533" "ENSMUSG00000022548" "ENSMUSG00000061740" "ENSMUSG00000050063" ...
## $ external_synonym : chr "2510006M18Rik" NA "2D22" "Bssp" ...
## $ chromosome_name : chr "5" "16" "15" "7" ...
## $ gene_biotype : chr "protein_coding" "protein_coding" "protein_coding" "protein_coding" ...
## $ phenotype_description : chr "abnormal circulating amino acid level" "abnormal lipid homeostasis" "abnormal skin morphology" "abnormal cytokine level" ...
## $ hsapiens_homolog_associated_gene_name: chr "ASL" "APOD" "CYP2D6" "KLK6" ...
data.frame
Objects
We already saw how the functions head()
and str()
can be useful to
check the content and the structure of a data frame. Here is a
non-exhaustive list of functions to get a sense of the
content/structure of the data. Let’s try them out!
Size:
dim(rna)
- returns a vector with the number of rows in the first
element, and the number of columns as the second element (the
dimensions of the object)nrow(rna)
- returns the number of rowsncol(rna)
- returns the number of columnsContent:
head(rna)
- shows the first 6 rowstail(rna)
- shows the last 6 rowsNames:
names(rna)
- returns the column names (synonym of colnames()
for
data.frame
objects)rownames(rna)
- returns the row namesSummary:
str(rna)
- structure of the object and information about the
class, length and content of each columnsummary(rna)
- summary statistics for each columnNote: most of these functions are “generic”, they can be used on other types of
objects besides data.frame
.
► Question
Based on the output of str(rna)
, can you answer the following
questions?
rna
?
► Solution
Our rna
data frame has rows and columns (it has 2 dimensions), if we
want to extract some specific data from it, we need to specify the
“coordinates” we want from it. Row numbers come first, followed by
column numbers. However, note that different ways of specifying these
coordinates lead to results with different classes.
# first element in the first column of the data frame (as a vector)
rna[1, 1]
# first element in the 6th column (as a vector)
rna[1, 6]
# first column of the data frame (as a vector)
rna[, 1]
# first column of the data frame (as a data.frame)
rna[1]
# first three elements in the 7th column (as a vector)
rna[1:3, 7]
# the 3rd row of the data frame (as a data.frame)
rna[3, ]
# equivalent to head_rna <- head(rna)
head_rna <- rna[1:6, ]
head_rna
:
is a special function that creates numeric vectors of integers in
increasing or decreasing order, test 1:10
and 10:1
for
instance. See section 3.9 for details.
You can also exclude certain indices of a data frame using the “-
” sign:
rna[, -1] ## The whole data frame, except the first column
rna[-c(7:32428), ] ## Equivalent to head(rna)
Data frames can be subset by calling indices (as shown previously), but also by calling their column names directly:
rna["gene"] # Result is a data.frame
rna[, "gene"] # Result is a vector
rna[["gene"]] # Result is a vector
rna$gene # Result is a vector
In RStudio, you can use the autocompletion feature to get the full and correct names of the columns.
When we inspect the elements of the column
hsapiens_homolog_associated_gene_name
(for example with View(rna)
),
we can see that some cells contain NA values. If we wanted to extract
only mouse genes of this table that have a human homologous,
we could combine is.na()
and data frames subsetting:
is_missing_hsapiens_homolog <- is.na(rna$hsapiens_homolog_associated_gene_name)
rna_hsapiens_homolog <- rna[!is_missing_hsapiens_homolog,]
## gene sample expression organism age sex infection strain
## 1 Asl GSM2545336 1170 Mus musculus 8 Female InfluenzaA C57BL/6
## 2 Apod GSM2545336 36194 Mus musculus 8 Female InfluenzaA C57BL/6
## 3 Cyp2d22 GSM2545336 4060 Mus musculus 8 Female InfluenzaA C57BL/6
## 4 Klk6 GSM2545336 287 Mus musculus 8 Female InfluenzaA C57BL/6
## 5 Fcrls GSM2545336 85 Mus musculus 8 Female InfluenzaA C57BL/6
## time tissue mouse ENTREZID
## 1 8 Cerebellum 14 109900
## 2 8 Cerebellum 14 11815
## 3 8 Cerebellum 14 56448
## 4 8 Cerebellum 14 19144
## 5 8 Cerebellum 14 80891
## product
## 1 argininosuccinate lyase, transcript variant X1
## 2 apolipoprotein D, transcript variant 3
## 3 cytochrome P450, family 2, subfamily d, polypeptide 22, transcript variant 2
## 4 kallikrein related-peptidase 6, transcript variant 2
## 5 Fc receptor-like S, scavenger receptor, transcript variant X1
## ensembl_gene_id external_synonym chromosome_name gene_biotype
## 1 ENSMUSG00000025533 2510006M18Rik 5 protein_coding
## 2 ENSMUSG00000022548 <NA> 16 protein_coding
## 3 ENSMUSG00000061740 2D22 15 protein_coding
## 4 ENSMUSG00000050063 Bssp 7 protein_coding
## 5 ENSMUSG00000015852 2810439C17Rik 3 protein_coding
## phenotype_description
## 1 abnormal circulating amino acid level
## 2 abnormal lipid homeostasis
## 3 abnormal skin morphology
## 4 abnormal cytokine level
## 5 decreased CD8-positive alpha-beta T cell number
## hsapiens_homolog_associated_gene_name
## 1 ASL
## 2 APOD
## 3 CYP2D6
## 4 KLK6
## 5 FCRL2
## [ reached 'max' / getOption("max.print") -- omitted 1 rows ]
## [1] FALSE
► Question
How many mouse genes do not have a human homologous?
► Solution
► Question
Create a data.frame
(rna_200
) containing only the data in
row 200 of the rna
dataset.
Notice how nrow()
gave you the number of rows in a data.frame
?
Use that number to pull out just that last row in the initial
rna
data frame.
Compare that with what you see as the last row using tail()
to
make sure it’s meeting expectations.
Pull out that last row using nrow()
instead of the row number.
Create a new data frame (rna_last
) from that last row.
Use nrow()
to extract the row that is in the middle of the
rna
dataframe. Store the content of this row in an object
named rna_middle
.
Combine nrow()
with the -
notation above to reproduce the
behavior of head(rna)
, keeping just the first through 6th
rows of the rna dataset.
► Solution
We have seen how to read a text-based spreadsheet into R using the
read.table
family of functions. To export a data.frame
to a
text-based spreadsheet, we can use the write.table
set of functions
(write.csv
, write.delim
, …). They all take the variable to be
exported and the file to be exported to. For example, to export the
rna
data to the my_rnaseq.csv
file in the data_output
directory, we would execute:
This new csv file can now be shared with other collaborators who aren’t familiar with R.
Factors represent categorical data. They are stored as integers associated with labels and they can be ordered or unordered. While factors look (and often behave) like character vectors, they are actually treated as integer vectors by R. So you need to be very careful when treating them as strings.
Once created, factors can only contain a pre-defined set of values, known as levels. By default, R always sorts levels in alphabetical order. For instance, if you have a factor with 2 levels:
R will assign 1
to the level "female"
and 2
to the level
"male"
(because f
comes before m
, even though the first element
in this vector is "male"
). You can see this by using the function
levels()
and you can find the number of levels using nlevels()
:
## [1] "female" "male"
## [1] 2
► Question
► Solution
Sometimes, the order of the factors does not matter, other times you
might want to specify the order because it is meaningful (e.g., “low”,
“medium”, “high”), it improves your visualization, or it is required
by a particular type of analysis. Here, one way to reorder our levels
in the sex
vector would be:
## [1] male female female male female
## Levels: female male
## [1] male female female male female
## Levels: male female
In R’s memory, these factors are represented by integers (1, 2, 3),
but are more informative than integers because factors are self
describing: "female"
, "male"
is more descriptive than 1
,
2
. Which one is “male”? You wouldn’t be able to tell just from the
integer data. Factors, on the other hand, have this information built
in. It is particularly helpful when there are many levels (like the
species names in our example dataset).
If you need to convert a factor to a character vector, you use
as.character(x)
.
## [1] "male" "female" "female" "male" "female"
When your data is stored as a factor, you can use the plot()
function to get a quick glance at the number of observations
represented by each factor level. Let’s look at the number of males
and females in our data.
If we want to rename these factor, it is sufficient to change its levels:
## [1] "male" "female"
## [1] M F F M F
## Levels: M F
► Question
► Question
We have seen how data frames are created when using read.csv()
, but
they can also be created by hand with the data.frame()
function.
There are a few mistakes in this hand-crafted data.frame
. Can you
spot and fix them? Don’t hesitate to experiment!
animal_data <- data.frame(
animal = c(dog, cat, sea cucumber, sea urchin),
feel = c("furry", "squishy", "spiny"),
weight = c(45, 8 1.1, 0.8))
► Solution
► Question
Can you predict the class for each of the columns in the following example?
Check your guesses using str(country_climate)
:
Are they what you expected? Why? Why not?
Try again by adding stringsAsFactors = TRUE
after the last
variable when creating the data frame? What is happening now?
stringsAsFactors
can also be set when reading text-based
spreadsheets into R using read.csv()
.
country_climate <- data.frame(
country = c("Canada", "Panama", "South Africa", "Australia"),
climate = c("cold", "hot", "temperate", "hot/temperate"),
temperature = c(10, 30, 18, "15"),
northern_hemisphere = c(TRUE, TRUE, FALSE, "FALSE"),
has_kangaroo = c(FALSE, FALSE, FALSE, 1)
)
The automatic conversion of data type is sometimes a blessing, sometimes an annoyance. Be aware that it exists, learn the rules, and double check that data you import in R are of the correct type within your data frame. If not, use it to your advantage to detect mistakes that might have been introduced during data entry (a letter in a column that should only contain numbers for instance).
Learn more in this RStudio tutorial
Before proceeding, now that we have learnt about dataframes, let’s
recap package installation and learn about a new data type, namely the
matrix
. Like a data.frame
, a matrix has two dimensions, rows and
columns. But the major difference is that all cells in a matrix
must
be of the same type: numeric
, character
, logical
, … In that
respect, matrices are closer to a vector
than a data.frame
.
The default constructor for a matrix is matrix
. It takes a vector of
values to populate the matrix and the number of row and/or
columns9 Either the number of rows or columns are enough, as the other
one can be deduced from the length of the values. Try out what happens
if the values and number of rows/columns don’t add up.. The values are sorted along the columns, as illustrated
below but you can also sort them along the row with the argument byrow = TRUE
.
## [,1] [,2] [,3]
## [1,] 1 4 7
## [2,] 2 5 8
## [3,] 3 6 9
► Question
Using the function installed.packages()
, create a character
matrix containing the information about all packages currently installed on your computer. Explore it.
► Solution
It is often useful to create large random data matrices as test
data. The exercise below asks you to create such a matrix with random
data drawn from a normal distribution of mean 0 and standard deviation
1, which can be done with the rnorm()
function.
► Question
Construct a matrix of dimension 1000 by 3 of normally distributed data (mean 0, standard deviation 1).
► Solution
One of the most common issues that new (and experienced!) R users have is converting date and time information into a variable that is appropriate and usable during analyses.
Dates in spreadsheets are generally stored in a single column. While this seems the most natural way to record dates, it actually is not best practice. A spreadsheet application will display the dates in a seemingly correct way (to a human observer) but how it actually handles and stores the dates may be problematic. It is often much safer to store dates with YEAR, MONTH and DAY in separate columns or as YEAR and DAY-OF-YEAR in separate columns.
Spreadsheet programs such as LibreOffice, Microsoft Excel, OpenOffice, Gnumeric, … have different (and often incompatible) ways of encoding dates (even for the same program between versions and operating systems). Additionally, Excel can turn things that aren’t dates into dates (Zeeberg et al. (2004Zeeberg, Barry R., Joseph Riss, David W. Kane, Kimberly J. Bussey, Edward Uchio, W. Marston Linehan, J. Carl Barrett, and John N. Weinstein. 2004. “Mistaken Identifiers: Gene Name Errors Can Be Introduced Inadvertently When Using Excel in Bioinformatics.” BMC Bioinformatics 5 (1): 80. https://doi.org/10.1186/1471-2105-5-80.)), for example names or identifiers like MAR1, DEC1, OCT4. So if you’re avoiding the date format overall, it’s easier to identify these issues.
The Dates as data section of the Data Carpentry lesson provides additional insights about pitfalls of dates with spreadsheets.
We are going to use the ymd()
function from the package
lubridate
(that belongs to the tidyverse
, which we’ll
focus on in the next chapter). lubridate
gets installed as part
as the tidyverse
installation. Let’s load it with
ymd()
takes a vector representing year, month, and day, and converts
it to a Date
vector. Date
is a class of data recognized by R as
being a date and can be manipulated as such. The argument that the
function requires is flexible, but, as a best practice, is a character
vector formatted as “YYYY-MM-DD”.
Let’s create a date object and inspect its structure:
## Date[1:1], format: "2015-01-01"
Now let’s paste the year, month, and day separately - we get the same result:
# sep indicates the character to use to separate each component
my_date <- ymd(paste("2015", "1", "1", sep = "-"))
str(my_date)
## Date[1:1], format: "2015-01-01"
Let’s now familiarise ourselves with a typical date manipulation
pipeline. The small data below has stored dates in different year
,
month
and day
columns.
x <- data.frame(year = c(1996, 1992, 1987, 1986, 2000, 1990, 2002, 1994, 1997, 1985),
month = c(2, 3, 3, 10, 1, 8, 3, 4, 5, 5),
day = c(24, 8, 1, 5, 8, 17, 13, 10, 11, 24),
value = c(4, 5, 1, 9, 3, 8, 10, 2, 6, 7))
x
## year month day value
## 1 1996 2 24 4
## 2 1992 3 8 5
## 3 1987 3 1 1
## 4 1986 10 5 9
## 5 2000 1 8 3
## 6 1990 8 17 8
## 7 2002 3 13 10
## 8 1994 4 10 2
## 9 1997 5 11 6
## 10 1985 5 24 7
Now we apply this function to the x
dataset. We first dreate a
character vector from the year
, month
, and day
columns of x
using paste()
:
## [1] "1996-2-24" "1992-3-8" "1987-3-1" "1986-10-5" "2000-1-8" "1990-8-17"
## [7] "2002-3-13" "1994-4-10" "1997-5-11" "1985-5-24"
This character vector can be used as the argument for ymd()
:
## [1] "1996-02-24" "1992-03-08" "1987-03-01" "1986-10-05" "2000-01-08"
## [6] "1990-08-17" "2002-03-13" "1994-04-10" "1997-05-11" "1985-05-24"
The resulting Date
vector can be added to x
as a new column called date
:
x$date <- ymd(paste(x$year, x$month, x$day, sep = "-"))
str(x) # notice the new column, with 'date' as the class
## 'data.frame': 10 obs. of 5 variables:
## $ year : num 1996 1992 1987 1986 2000 ...
## $ month: num 2 3 3 10 1 8 3 4 5 5
## $ day : num 24 8 1 5 8 17 13 10 11 24
## $ value: num 4 5 1 9 3 8 10 2 6 7
## $ date : Date, format: "1996-02-24" "1992-03-08" ...
Let’s make sure everything worked correctly. One way to inspect the
new column is to use summary()
:
## Min. 1st Qu. Median Mean 3rd Qu.
## "1985-05-24" "1988-01-11" "1993-03-24" "1993-03-18" "1997-01-20"
## Max.
## "2002-03-13"
Note that ymd()
expects to have the year, month and day, in that
order. If you have for instance day, month and year, you would need
dmy()
.
## [1] "2002-02-24" "2003-03-08" "2003-03-01" "2010-10-05" "2001-01-08"
## [6] "2008-08-17" "2003-03-13" "2004-04-10" "2005-05-11" "2005-05-24"
lubdridate
has many functions to address all date variations.
A data type that we haven’t seen yet, but that is useful to know are lists:
list
: one dimension, every item can be of a different data
type.Below, let’s create a list containing a vector of numbers, characters, a matrix, a dataframe and another list:
l <- list(1:10, ## numeric
letters, ## character
installed.packages(), ## a matrix
cars, ## a data.frame
list(1, 2, 3)) ## a list
length(l)
## [1] 5
## List of 5
## $ : int [1:10] 1 2 3 4 5 6 7 8 9 10
## $ : chr [1:26] "a" "b" "c" "d" ...
## $ : chr [1:776, 1:16] "abind" "affy" "affyio" "annotate" ...
## ..- attr(*, "dimnames")=List of 2
## .. ..$ : chr [1:776] "abind" "affy" "affyio" "annotate" ...
## .. ..$ : chr [1:16] "Package" "LibPath" "Version" "Priority" ...
## $ :'data.frame': 50 obs. of 2 variables:
## ..$ speed: num [1:50] 4 4 7 7 8 9 10 10 10 11 ...
## ..$ dist : num [1:50] 2 10 4 22 16 10 18 26 34 17 ...
## $ :List of 3
## ..$ : num 1
## ..$ : num 2
## ..$ : num 3
List subsetting is done using []
to subset a new sub-list or [[]]
to extract a single element of that list (using indices or names, of
the list is named).
## [1] 1 2 3 4 5 6 7 8 9 10
## [[1]]
## [1] 1 2 3 4 5 6 7 8 9 10
##
## [[2]]
## [1] "a" "b" "c" "d" "e" "f" "g" "h" "i" "j" "k" "l" "m" "n" "o" "p" "q" "r"
## [19] "s" "t" "u" "v" "w" "x" "y" "z"
## [[1]]
## [1] 1 2 3 4 5 6 7 8 9 10
► Question
You can also attribute a name to each element of a list. Give the
following names (in that order) to the list elements with the function
names()
: "numbers"
, "alphabet"
, "installed_packages"
, "cars"
and "random"
. Check if the names were correctly attributed.
► Solution
► Question
Subset the previously defined list l
, to keep:
cars
data.framecars
data.frame
► Solution
So far, we have seen several types of R object varying in the number of dimensions and whether they could store a single or multiple data types:
vector
: one dimension (they have a length), single type of data.matrix
: two dimensions, single type of data.data.frame
: two dimensions, one type per column.list
: one dimension (length), any type per element.► Question
You’re doing an colony counting experiment, counting every day how many molds you see in your cell cultures.
Create a vector named molds
containing the results of your counts:
1, 2, 5, 8 and 10. Create a vector days
containing the week day,
from Monday to Friday. Use these two vector to create a data.frame
named molds_study
containing two variables, Day
and
Molds_count
.
Create a new data.frame
that contains the observations where more
than 2 colonies were counted. How many observations are there? How
many counts are there in total for these observations.
You repeat the molds study experiment the following week and count the following numbers of molds: 1, 6, 6, 5 and 4.
Add these data as a third column to the molds_study
data.frame
and rename the variables as Day
, Molds_1
and Molds_2
.
Calculate for each experiment the total number of molds counted. Check if the first experiment counted more molds than the second one.
Save the molds_study
variable in a file named molds_study.rda
.
► Question
We are going to analyse beer consumption in 48 individuals. The data
are available in the rWSBIM1207
package. The data illustrated the
fictive beer consumption in liters per year at different age according
to gender and employment.
Load the rWSBIM1207
package. If the package isn’t installed of its
version is greater than 0.1.1, install it from the
UCLouvain-CBIO/rWSBIM1207
GitHub repository using the
BiocManager::install()
(or remotes::install_github()
)
function. If you use a recent Renku enironment, the package is
already available.
Using the beers.csv()
function from rWSBIM1207
, find the path
the beers.csv
file and read it to produce a data.frame
named
beers
. The spreadsheet uses semi-colons ;
to separate cells. Use
read.csv2()
and read.delim()
and set the separator
appropriately, and verify that the two variables are identical.
Check the number of observations and identify the variables that are
available. Calculate a summary of each variable using the summary
function directly on the data.frame
.
Calculate the mean and the median age and consumption.
Do men consume more beer than women on average? To answer this
question, calculate the mean consumption for men only, selecting the
observations with Gender
equal to Male
. Then do the same for
observations with Gender
equal to Female
.
Using the table()
function, generate a two-way table of gender and
employment status.
Remove observations with missing values and export the data into a
new csv
file called beers_no_na.csv
.
► Question
We are going to analyse clinical data from The Cancer Genome Atlas
(TCGA). The data are available in the rWSBIM1207
package.
Load the rWSBIM1207
package. If the package isn’t installed of its
version is greater than 0.1.1, install it from the
UCLouvain-CBIO/rWSBIM1207
GitHub repository using the
BiocManager::install()
(or remotes::install_github()
)
functions. If you use a recent Renku enironment, the package is
already available.
Obtain the path to the csv file containing the clinical data need for
this exercise using the clinical1.csv
function and read it into R
as a data.frame
called clinical
.
Inspect the data using str
and View
. How many patients are
recorded in the table?
Print the column names using two different functions.
Create a smaller data frame called clinical_mini
containing only
the columns corresponding to the patientID
, gender
,
age_at_diagnosis
and smoking_history
. Try to do this using
column indices and column names.
Inspect the smoking_history
column. How many categories are
recorded? How many observations are there for each category?
The column age at diagnosis is recorded in days. Create a new column
years_at_diagnosis
corresponding to the age at diagnosis converted
in years.
Calculate the mean and median age at diagnosis. Hint: pay attention to missing values!
Is there a difference between the years_at_diagnosis
for male and
female patients?
Use the quantile
function to calculate the first and last quartile
of age at diagnosis. Use the help function (?quantile
) to see how
to use the quantile
function.
Use the summary
function to confirm your previous results.
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