<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Campbell IM</submitter><funding>NINDS NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>3387-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4274347</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(23)</volume><pubmed_abstract>&lt;h4>Motivation&lt;/h4>Set-based network similarity metrics are increasingly used to productively analyze genome-wide data. Conventional approaches, such as mean shortest path and clique-based metrics, have been useful but are not well suited to all applications. Computational scientists in other disciplines have developed communicability as a complementary metric. Network communicability considers all paths of all lengths between two network members. Given the success of previous network analyses of protein-protein interactions, we applied the concepts of network communicability to this problem. Here we show that our communicability implementation has advantages over traditional approaches. Overall, analyses suggest network communicability has considerable utility in analysis of large-scale biological networks.&lt;h4>Availability and implementation&lt;/h4>We provide our method as an R package for use in both human protein-protein interaction network analyses and analyses of arbitrary networks along with a tutorial at http://www.shawlab.org/NetComm/.</pubmed_abstract><journal>Bioinformatics (Oxford, England)</journal><pubmed_title>NetComm: a network analysis tool based on communicability.</pubmed_title><pmcid>PMC4274347</pmcid><funding_grant_id>R25 GM056929</funding_grant_id><funding_grant_id>K12 GM084897</funding_grant_id><funding_grant_id>T32 GM007330</funding_grant_id><funding_grant_id>F31 NS083159</funding_grant_id><pubmed_authors>Campbell IM</pubmed_authors><pubmed_authors>Shaw CA</pubmed_authors><pubmed_authors>Chen ES</pubmed_authors><pubmed_authors>James RA</pubmed_authors></additional><is_claimable>false</is_claimable><name>NetComm: a network analysis tool based on communicability.</name><description>&lt;h4>Motivation&lt;/h4>Set-based network similarity metrics are increasingly used to productively analyze genome-wide data. Conventional approaches, such as mean shortest path and clique-based metrics, have been useful but are not well suited to all applications. Computational scientists in other disciplines have developed communicability as a complementary metric. Network communicability considers all paths of all lengths between two network members. Given the success of previous network analyses of protein-protein interactions, we applied the concepts of network communicability to this problem. Here we show that our communicability implementation has advantages over traditional approaches. Overall, analyses suggest network communicability has considerable utility in analysis of large-scale biological networks.&lt;h4>Availability and implementation&lt;/h4>We provide our method as an R package for use in both human protein-protein interaction network analyses and analyses of arbitrary networks along with a tutorial at http://www.shawlab.org/NetComm/.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Dec</publication><modification>2021-02-21T01:26:30Z</modification><creation>2019-03-27T01:42:14Z</creation></dates><accession>S-EPMC4274347</accession><cross_references><pubmed>25123899</pubmed><doi>10.1093/bioinformatics/btu536</doi></cross_references></HashMap>