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The increasing wealth of transcriptomic data and current computational tools enable to infer how protein interactomes and complexomes may be assembled in specific samples. With CompleXChange this information can be exploited to conduct differential analyses of the dynamic protein complexome in a quantitative manner.
The corresponding publication can be found on https://doi.org/10.1186/s12859-019-2852-z.
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GNU General Public License version 3.0 (GPLv3)Follow CompleXChange
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