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Custom datasets are created and visualized in the analysis section (click on the Analysis tab above). On most pages you will find bracketed question mark [?] that you can mouse over for context specific help. Below is a general help description of the analysis section of the M3D website.
To begin creating a custom dataset, click the Analysis tab at the top of the webpage. You begin by choosing a compendium. Higher build numbers for a species indicate more recent builds. Typically, you'll want to use the compendium with the highest build number for your species of interest. Older databases are maintained so that analyses performed on
these data can be repeated if necessary (this is important, because some of the normalization types
use the data from all of the chips to determine an expression value for a gene, so as arrays are added to the dataset the value for
past experiments change a little).
After choosing a database, you are presented with a small table that allows you to change
to a new compendium. This table also contains statistics describing your current dataset including the number of genes and experiments in your current dataset. In this table, you can click the links to add genes or experiments. If you currently have 0 genes or 0 experiments in your dataset, you will automatically be taken to pages for adding genes and experiments.
Experiments can be selected individually or as projects. Projects are groups of experiments run together. Typically projects are the data used for one scientific publication. An experiment represents one specific condition and may have replicates. Currently, it is not possible to select individual chips.
Once you have a dataset with at least one gene and at least one experiment, you can visualize or download the dataset.
M3D provides several different visualizations. The best way to see what they do is to try them with small datasets.
Visualization of large datasets (> 500 genes) is rather slow due to the time
required to read all of the expression information from the database for each analysis.
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