Skip to content
Snippets Groups Projects
Commit ae4d7532 authored by Andrzej Oles's avatar Andrzej Oles
Browse files

Edits to the short and detailed descriptions of the practical

parent b144b027
No related branches found
No related tags found
1 merge request!1Edits to the short and detailed descriptions of the practical
# Short description of the practical
P12 Data handling and visual exploration of the processed and scored data from P3 / P9
P12 Data handling and visual exploration of the processed and scored data from P10
(ATC, Flex Lab B)
......@@ -10,39 +10,37 @@ Staff: Andrzej Oles, Mike Smith, Bernd Klaus
Work:
1. Importing the data into R, the concept of "tidy data", introduction
to data handling strategies
2. Visual exploration of data using quality-control related plots, e.g. heatmaps,
2. Visual exploration of data using quality control related plots, e.g. heatmaps
and PCA plots
# Short description of the practical
# Detailed description of the practical
High-throughput microscopy screens with technologies such as RNAi, CRISPR-Cas
and libraries of drug compounds typically generate large quantities of data that
and libraries of drug compounds generate large amounts of data that
are potentially rich in biological information. Typically thousands of gene or
drug targets are screened and tens or even hundreds of image features are
extracted. Exploring these large datasets is challenging. R packages from
the "tidyverse" will lead the way here.
In the tutorial we will fist introduce the concept of "tidy data" that provides
a practically useful way of organizing big experimental datasets
and show how turning the initial data in to a "tidy" representation.
extracted. Finding patterns indicative of exciting biology within these large
datasets and prioritizing lists of candidate hits for further experimental
testing is challenging, even after rigorous quality control steps and correction
for technical biases have been performed.
In this tutorial we will first introduce the concept of "tidy data", which provides
a practically useful way of organizing big datasets,
and show how to turn the initial data into a "tidy" representation.
We will then demonstrate how to perform large-scale visualization of the screen
results and show how to use this to explore patterns in the data.
Methods such as Principal component analysis (PCA) and clustering will be
employed and the participants will be introduced to the advanced graphical
results, and how to apply this to explore patterns in the data.
Methods such as principal component analysis (PCA) and clustering will be
employed, and the participants will be introduced to the advanced graphical
capabilities of R.
We will work on the cell-classification results from labs P3 / P9, so this
this lab will lead the way to hit calling
strategies and comprehensive downstream analyses.
We will perform all analyses using open source R/Bioconductor software.
We will work on the cell classification results from practical P10, so this
tutorial will lead the way to hit calling
strategies and comprehensive downstream analysis.
All analyses will be performed in open source R/Bioconductor software.
Software:
......
0% Loading or .
You are about to add 0 people to the discussion. Proceed with caution.
Finish editing this message first!
Please register or to comment