Project organization is one of the most important parts of a sequencing project, but is often overlooked in the excitement to get a first look at new data. While it’s best to get yourself organized before you begin analysis, it’s never too late to start.
You should approach your sequencing project in a very similar way to how you do a biological experiment, and ideally, begins with experimental design. We’re going to assume that you’ve already designed a beautiful sequencing experiment to address your biological question, collected appropriate samples, and that you have enough statistical power. For all of those steps, collecting specimens, extracting DNA, prepping your samples, you’ve likely kept a lab notebook that details how and why you did each step, but documentation doesn’t stop at the sequencer!
Every computational analysis you do is going to spawn many files, and inevitability, you’ll want to run some of those analysis again. Genomics projects can quickly accumulates hundreds of files across tens of folders. Do you remember what PCR conditions you used to create your sequencing library? Probably not. Similarly, you probably won’t remember whether your best alignment results were in Analysis1, AnalysisRedone, or AnalysisRedone2; or which quality cutoff you used.
Luckily, recording your computational experiments is even easier than recording lab data. Copy/Paste will become your best friend, sensible file names will make your analysis traversable by you and your collaborators, and writing the methods section for your next paper will be a breeze. Let’s look at the best practices for documenting your genomics project.
Your future self will thank you.
In this exercise we will setup a filesystem for the project we will be using over the next few days. We will also introduce you to some helpful shell commands/programs/tools:
mkdir
history
tail
|
nano
>>
Inspired by the guide below, we will start by create a directory that we can use for the rest of the workshop:
First, make sure that you are in your home directory:
bash
$ pwd
/home/dcuser
# Hopefully you got the above output '/home/dcuser'
Tip: Remember, when we give a command, rather than copying and pasting, just type it out. Also the ‘$’ indicates we are at the command prompt, do not include that in your command.
Tip If you were not in your home directory, the easiest way to get there is to enter the command cd
which always returns you to home.
Next, try making the following directories using the mkdir
command
Verify that you have created the directories;
bash
$ ls -R dc_workshop
if you have created these directories, you should get the following output from that command:
```bash dc_workshop/: data docs results
dc_workshop/data:
dc_workshop/docs:
dc_workshop/results: ```
The history command is a convenient way to document the all the commands you have used while analyzing and manipulating your project. Let’s document the work we have done to create these folders.
View the commands that you have used so far during this session using history
:
bash
$ history
The history likely contains many more commands that you have used just for these projects. Let’s view the last several commands so that focus on just what we need for the project.
View the last n lines of your history (where n = approximately the last few lines you think relevant - for our example we will use the last 7:
bash
$ history | tail -n7
As you may remember from the shell lesson, the pipe |
sends the output of history to the next program, in this case, tail. We have used the -n option to give the last 7 lines.
>>
to create a file called dc_workshop_log_XXXX_XX_XX.txt (Use the four-digit year, two-digit month, and two digit day, e.g. dc_workshop_log_2015_07_30.txt)history
command itself. To remove this redundancy from our log, lets use the nano
text editor to fix the file:
bash
$ nano dc_workshop_log
From the nano screen, you should be able to use your cursor to navigate, type, and delete any redundant lines.
# 2015_07_30
# Created sample directories for the Data Carpentry workshop
mv
command. Questions:
1. What is the default number of lines that tail displays?
2. What is the difference between ‘>’ and ‘»’
[A Quick Guide to Organizing Computational Biology Projects] (http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1000424)