1-DAV-202 Data Management 2023/24
Previously 2-INF-185 Data Source Integration
Difference between revisions of "Lr1"
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Program for this lecture: basics of R | Program for this lecture: basics of R | ||
− | * very short | + | * A very short introduction will be given as a lecture. |
− | * | + | * Exercises have the form of a tutorial: read a bit of text, try some commands, extend/modify them as requested in individual tasks |
In this course we cover several languages popular for scripting and data processing: Perl, Python, R. | In this course we cover several languages popular for scripting and data processing: Perl, Python, R. | ||
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==Gene expression data== | ==Gene expression data== | ||
− | * DNA | + | * DNA molecules contain regions called genes, which "recipes" for making proteins |
* Gene expression is the process of creating a protein according to the "recipe" | * Gene expression is the process of creating a protein according to the "recipe" | ||
* It works in two stages: first a gene is copied (transcribed) from DNA to RNA, then translated from RNA to protein | * It works in two stages: first a gene is copied (transcribed) from DNA to RNA, then translated from RNA to protein | ||
Line 68: | Line 68: | ||
* Downloaded from the [https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE5926 GEO database] | * Downloaded from the [https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE5926 GEO database] | ||
* Data was preprocessed: normalized, converted to logarithmic scale | * Data was preprocessed: normalized, converted to logarithmic scale | ||
− | * Only 1220 genes with biggest changes in expression are included in our dataset | + | * Only 1220 genes with the biggest changes in expression are included in our dataset |
* Gene expression measurements under 5 conditions: | * Gene expression measurements under 5 conditions: | ||
** Control: yeast grown in a normal environment | ** Control: yeast grown in a normal environment | ||
Line 74: | Line 74: | ||
* From each condition (reference and each acid) we have 3 replicates, together 15 experiments | * From each condition (reference and each acid) we have 3 replicates, together 15 experiments | ||
* The goal is to observe how the acids influence the yeast and the activity of its genes | * The goal is to observe how the acids influence the yeast and the activity of its genes | ||
− | Part of the file (only first 4 experiments and first 3 genes shown), strings 2mic_D_protein, AAC3, AAD15 are identifiers of genes | + | Part of the file (only first 4 experiments and first 3 genes shown), strings <tt>2mic_D_protein, AAC3, AAD15</tt> are identifiers of genes |
<pre> | <pre> | ||
,control1,control2,control3,acetate1,acetate2,acetate3,... | ,control1,control2,control3,acetate1,acetate2,acetate3,... |
Revision as of 13:36, 8 April 2021
Program for this lecture: basics of R
- A very short introduction will be given as a lecture.
- Exercises have the form of a tutorial: read a bit of text, try some commands, extend/modify them as requested in individual tasks
In this course we cover several languages popular for scripting and data processing: Perl, Python, R.
- Their capabilities overlap, many extensions emulate strengths of one in another.
- Choose a language based on your preference, level of knowledge, existing code for the task, the rest of the team.
- Quickly learn a new language if needed.
- Also possibly combine, e.g. preprocess data in Perl or Python, then run statistical analyses in R, automate the entire pipeline with bash or make.
Introduction
- R is an open-source system for statistical computing and data visualization
- Programming language, command-line interface
- Many built-in functions, additional libraries
- For example Bioconductor for bioinformatics
- We will concentrate on useful commands rather than language features
Working in R
Option 1: Run command R, type commands in a command-line interface
- It supports history of commands (arrows, up and down, Ctrl-R) and completing command names with the tab key
Option 2: Write a script to a file, run it from the command-line as follows:
R --vanilla --slave < file.R
Option 3: Use rstudio command to open a graphical IDE
- Sub-windows with editor of R scripts, console, variables, plots
- Ctrl-Enter in editor executes the current command in console
- You can also install RStudio on your home computer and work there
Option 4: If you like Jupyter notebooks, you can use them also to run R code, see for example an explanation of how to enable it in Google Colab [1].
In R, you can easily create plots. In command-line interface these open as a separate window, in Rstudio they open in one of the sub-windows.
x = c(1:10)
plot(x, x * x)
Suggested workflow
- Work interactively in Rstudio, notebook or on command line, try various options.
- Select useful commands, store in a script.
- Run the script automatically on new data/new versions, potentially as a part of a bigger pipeline.
Additional information
- Official tutorial
- Seefeld, Linder: Statistics Using R with Biological Examples (pdf book)
- Patrick Burns: The R Inferno (intricacies of the language)
- Other books
- Built-in help: ? plot displays help for plot command
Gene expression data
- DNA molecules contain regions called genes, which "recipes" for making proteins
- Gene expression is the process of creating a protein according to the "recipe"
- It works in two stages: first a gene is copied (transcribed) from DNA to RNA, then translated from RNA to protein
- Different proteins are created in different quantities and their amount depends on the needs of a cell
- There are several technologies (microarray, RNA-seq) for measuring the amount of RNA for individual genes, this gives us some measure how active each gene is under given circumstances
Gene expression data
- Rows: genes
- Columns: experiments (e.g. different conditions or different individuals)
- Each value is the expression of a gene, i.e. the relative amount of mRNA for this gene in the sample
We will use a data set for yeast:
- Abbott, Derek A., et al. "Generic and specific transcriptional responses to different weak organic acids in anaerobic chemostat cultures of Saccharomyces cerevisiae." FEMS yeast research 7.6 (2007): 819-833.
- Downloaded from the GEO database
- Data was preprocessed: normalized, converted to logarithmic scale
- Only 1220 genes with the biggest changes in expression are included in our dataset
- Gene expression measurements under 5 conditions:
- Control: yeast grown in a normal environment
- 4 different acids added so that cells grow 50% slower (acetic, propionic, sorbic, benzoic)
- From each condition (reference and each acid) we have 3 replicates, together 15 experiments
- The goal is to observe how the acids influence the yeast and the activity of its genes
Part of the file (only first 4 experiments and first 3 genes shown), strings 2mic_D_protein, AAC3, AAD15 are identifiers of genes
,control1,control2,control3,acetate1,acetate2,acetate3,... 2mic_D_protein,1.33613934199651,1.13348900359964,1.2726678684356,1.42903234691804,... AAC3,0.558482767397578,0.608410781454015,0.6663002997292,0.231622581964063,... AAD15,-0.927871996497105,-1.04072379902481,-1.01885986692013,-2.62459941525552,...