Supplementary data should be awesome like this
Among many other things, I recently read the wide-scope and well disseminated paper by Beroukhim et al (a very very loaded et al!) titled “The landscape of somatic copy-number alteration across human cancers”. An impressive study of 3,131 cancer specimens from 26 histological types of which 158 regions of focal somatic copy-number alterations were found.
I could go into detail about this study but what I wanted to mention here was not necessarily about the potential candidate genes or their possible functional implications. I wanted to mention the awesome web application that was produced along with this study which allows folks like me (read lazy!) to go over their datasets with minimal effort.
The Broad Institute’s Tumorscape is a portal that allows one to browse/search through a database of copy number alterations across multiple cancer types. Basically the findings of the previously mentioned paper.
In my opinion, this is much better than having to go through the raw supplementary data. If I were interested in further pursuing any of the studies performed, I could download the supplementary data, but if I’m just interested in browsing the results of this paper, the Tumorscape makes it far more pleasant.
There is obviously an overhead related to producing this type of portal, however the sheer number of people working on this project and the amount of data produced definitely justified the creation of such a web application.
Sorry if the title of this post was a bit misleading, but hey… it should be awesome, right? :)







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