The combination of powerful statistics and instant visualization generates exciting results. For RNA-seq data the combination of statistical filtering on expression levels with filtering on genomic entities enables focused analysis.
One of cornerstones is the possibility to analyze data using a flexible and easy to use statistical framework. The user can select among the following statistical methods:
- two group comparison (t-test)
- multi group comparison (F-test) (ANOVA)
- linear regression
- quadratic regression
- rank regression
In addition to the methods above, filtering on Fold change and Difference are supported.
An Open API to R is integrated and opens up for use of a wide range of other statistical methods. The program is shipped with a range of tests, examples include Limma and Mann Whitney.
The inbuilt statistical framework (a general linear statistical model) supports the handling of eliminated factors, which means that you can remove batch effects, work with paired data or even more complex experimental set-ups.
Templates is the functionality used for scripting work-flows in the program. You can use built-in Templates as a quick start to standard analyses or write your own templates to simplify repetitive tasks. Templates is also the tool for integration the program into tool chains.
Survival analysis is supported with integrated statisitcal methods such as Hazard ratio calculations as well as visualizations in Kaplan-Meier plots.
With the NGS module and the NGS filters more options are available. Select which regions of the genome to analyze in the Genome browser, dynamically select if the regions should be restricted by read coverage, specific regions or if variants should be present or not.
Clustering is supported in several ways; either in a semi-supervised mode using PCA or t-SNE with Projection score and variance filtering or in an unsupervised mode using kmeans++.
The Build classifier and Classify machine learning functionality enables both the option to easy build classifiers based on models such as Support Vector Machines (SVM), Random Trees (RT) and kNN and to classify new samples.
To compare and enhance your findings use the integrated GSEA Workbench which is set-up using only a few mouse-clicks. It does not get easier.
By combining the right annotations with statistical methods, data selection tools, and the eliminated factors function, a very broad range of different experiment designs can be analyzed.
Qlucore Omics Explorer also supports analysis using:
- Hierarchical clustering
The Status panel will continuously show exactly what calculations that have been applied to your data.