Looking at Metadata

We are studying a population of Escherichia coli (designated Ara-3), which were propagated for more than 40,000 generations in a glucose-limited minimal medium. This medium was supplemented with citrate which E. coli cannot metabolize in the aerobic conditions of the experiment. Sequencing of the populations at regular time points reveals that spontaneous citrate-using mutants (Cit+) appeared at around 31,000 generations. This metadata describes information on the Ara-3 clones and the columns represent:

The metadata file required for this lesson can be downloaded directly here or viewed in Github.

• First, make sure you are in the correct working directory by typing getwd()
• Second, create a new subdirectory within this working directory called data
• Third, move the just-downloaded Ecoli_metadata.csv file into this data directory

You are now ready to load the data. We are going to use the R function read.csv() to load the data file into memory (as a data.frame):

metadata <- read.csv('data/Ecoli_metadata.csv')

This statement doesn’t produce any output because assignment doesn’t display anything. If we want to check that our data has been loaded, we can print the variable’s value: metadata

Alternatively, wrapping an assignment in parentheses will perform the assignment and display it at the same time.

(metadata <- read.csv('data/Ecoli_metadata.csv'))

##      sample generation   clade strain     cit       run genome_size
## 1    REL606          0    <NA> REL606 unknown                  4.62
## 2  REL1166A       2000 unknown REL606 unknown SRR098028        4.63
## 3    ZDB409       5000 unknown REL606 unknown SRR098281        4.60
## 4    ZDB429      10000      UC REL606 unknown SRR098282        4.59
## 5    ZDB446      15000      UC REL606 unknown SRR098283        4.66
## 6    ZDB458      20000 (C1,C2) REL606 unknown SRR098284        4.63
## 7   ZDB464*      20000 (C1,C2) REL606 unknown SRR098285        4.62
## 8    ZDB467      20000 (C1,C2) REL606 unknown SRR098286        4.61
## 9    ZDB477      25000      C1 REL606 unknown SRR098287        4.65
## 10   ZDB483      25000      C3 REL606 unknown SRR098288        4.59
## 11    ZDB16      30000      C1 REL606 unknown SRR098031        4.61
## 12   ZDB357      30000      C2 REL606 unknown SRR098280        4.62
## 13  ZDB199*      31500      C1 REL606   minus SRR098044        4.62
## 14   ZDB200      31500      C2 REL606   minus SRR098279        4.63
## 15   ZDB564      31500    Cit+ REL606    plus SRR098289        4.74
## 16   ZDB30*      32000      C3 REL606   minus SRR098032        4.61
## 17   ZDB172      32000    Cit+ REL606    plus SRR098042        4.77
## 18   ZDB158      32500      C2 REL606   minus SRR098041        4.63
## 19   ZDB143      32500    Cit+ REL606    plus SRR098040        4.79
## 20   CZB199      33000      C1 REL606   minus SRR098027        4.59
## 21   CZB152      33000    Cit+ REL606    plus SRR097977        4.80
## 22   CZB154      33000    Cit+ REL606    plus SRR098026        4.76
## 23    ZDB83      34000    Cit+ REL606   minus SRR098034        4.60
## 24    ZDB87      34000      C2 REL606    plus SRR098035        4.75
## 25    ZDB96      36000    Cit+ REL606    plus SRR098036        4.74
## 26    ZDB99      36000      C1 REL606   minus SRR098037        4.61
## 27   ZDB107      38000    Cit+ REL606    plus SRR098038        4.79
## 28   ZDB111      38000      C2 REL606   minus SRR098039        4.62
## 29 REL10979      40000    Cit+ REL606    plus SRR098029        4.78
## 30 REL10988      40000      C2 REL606   minus SRR098030        4.62

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():

head(metadata)

##     sample generation   clade strain     cit       run genome_size
## 1   REL606          0    <NA> REL606 unknown                  4.62
## 2 REL1166A       2000 unknown REL606 unknown SRR098028        4.63
## 3   ZDB409       5000 unknown REL606 unknown SRR098281        4.60
## 4   ZDB429      10000      UC REL606 unknown SRR098282        4.59
## 5   ZDB446      15000      UC REL606 unknown SRR098283        4.66
## 6   ZDB458      20000 (C1,C2) REL606 unknown SRR098284        4.63

We’ve just done two very useful things. 1. We’ve read our data in to R, so now we can work with it in R 2. We’ve created a data frame (with the read.csv command) the standard way R works with data.

What are data frames?

data.frame is the de facto data structure for most tabular data and what we use for statistics and plotting.

A data.frame is a collection of vectors of identical lengths. Each vector represents a column, and each vector can be of a different data type (e.g., characters, integers, factors). The str() function is useful to inspect the data types of the columns.

A data.frame can be created by the functions read.csv() or read.table(), in other words, when importing spreadsheets from your hard drive (or the web).

By default, data.frame converts (= coerces) columns that contain characters (i.e., text) into the factor data type. Depending on what you want to do with the data, you may want to keep these columns as character. To do so, read.csv() and read.table() have an argument called stringsAsFactors which can be set to FALSE:

Let’s now check the __str__ucture of this data.frame in more details with the function str():

str(metadata)

## 'data.frame':    30 obs. of  7 variables:
##  $ sample     : Factor w/ 30 levels "CZB152","CZB154",..: 7 6 18 19 20 21 22 23 24 25 ...
##  $ generation : int  0 2000 5000 10000 15000 20000 20000 20000 25000 25000 ...
##  $ clade      : Factor w/ 7 levels "(C1,C2)","C1",..: NA 7 7 6 6 1 1 1 2 4 ...
##  $ strain     : Factor w/ 1 level "REL606": 1 1 1 1 1 1 1 1 1 1 ...
##  $ cit        : Factor w/ 3 levels "minus","plus",..: 3 3 3 3 3 3 3 3 3 3 ...
##  $ run        : Factor w/ 30 levels "","SRR097977",..: 1 5 22 23 24 25 26 27 28 29 ...
##  $ genome_size: num  4.62 4.63 4.6 4.59 4.66 4.63 4.62 4.61 4.65 4.59 ...

Inspecting 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.

• Size:
  • dim() - returns a vector with the number of rows in the first element, and the number of columns as the second element (the __dim__ensions of the object)
  • nrow() - returns the number of rows
  • ncol() - returns the number of columns
• Content:
  • head() - shows the first 6 rows
  • tail() - shows the last 6 rows
• Names:
  • names() - returns the column names (synonym of colnames() for data.frame objects)
• rownames() - returns the row names
• Summary:
• str() - structure of the object and information about the class, length and content of each column
• summary() - summary statistics for each column

Note: most of these functions are “generic”, they can be used on other types of objects besides data.frame.

str(metadata)

## 'data.frame':    30 obs. of  7 variables:
##  $ sample     : Factor w/ 30 levels "CZB152","CZB154",..: 7 6 18 19 20 21 22 23 24 25 ...
##  $ generation : int  0 2000 5000 10000 15000 20000 20000 20000 25000 25000 ...
##  $ clade      : Factor w/ 7 levels "(C1,C2)","C1",..: NA 7 7 6 6 1 1 1 2 4 ...
##  $ strain     : Factor w/ 1 level "REL606": 1 1 1 1 1 1 1 1 1 1 ...
##  $ cit        : Factor w/ 3 levels "minus","plus",..: 3 3 3 3 3 3 3 3 3 3 ...
##  $ run        : Factor w/ 30 levels "","SRR097977",..: 1 5 22 23 24 25 26 27 28 29 ...
##  $ genome_size: num  4.62 4.63 4.6 4.59 4.66 4.63 4.62 4.61 4.65 4.59 ...