<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Iancu OD</submitter><funding>NCATS NIH HHS</funding><funding>NIMH NIH HHS</funding><pagination>29-37</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4460837</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>The current study examined the changes in striatal gene network structure induced by short-term selective breeding from a heterogeneous stock for haloperidol response. Brain (striatum) gene expression data were obtained using the Illumina WG 8.2 array, and the datasets from responding and non-responding selected lines were independently interrogated using a weighted gene coexpression network analysis (WGCNA). We detected several gene modules (groups of coexpressed genes) in each dataset; the membership of the modules was found to be largely concordant, and a consensus network was constructed. Further validation of the network topology showed that using approximately 35 samples is sufficient to reliably infer the transcriptome network. An in-depth analysis showed significant changes in network structure and gene connectivity associated with the selected lines; these changes were validated using a bootstrapping procedure. The most dramatic changes were associated with a gene module richly annotated with neurobehavioral traits. The changes in network connectivity were concentrated in the links between this module and the rest of the network, in addition to changes within the module; this observation is consistent with recent results in protein and metabolic networks. These results suggest that a network-based strategy will help identify the genetic factors associated with haloperidol response.</pubmed_abstract><journal>Genes, brain, and behavior</journal><pubmed_title>Gene networks and haloperidol-induced catalepsy.</pubmed_title><pmcid>PMC4460837</pmcid><funding_grant_id>R01 MH051372</funding_grant_id><funding_grant_id>MH 51372</funding_grant_id><funding_grant_id>UL1 TR000128</funding_grant_id><pubmed_authors>McWeeney S</pubmed_authors><pubmed_authors>Hitzemann R</pubmed_authors><pubmed_authors>Darakjian P</pubmed_authors><pubmed_authors>Iancu OD</pubmed_authors><pubmed_authors>Malmanger B</pubmed_authors><pubmed_authors>Walter NA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gene networks and haloperidol-induced catalepsy.</name><description>The current study examined the changes in striatal gene network structure induced by short-term selective breeding from a heterogeneous stock for haloperidol response. Brain (striatum) gene expression data were obtained using the Illumina WG 8.2 array, and the datasets from responding and non-responding selected lines were independently interrogated using a weighted gene coexpression network analysis (WGCNA). We detected several gene modules (groups of coexpressed genes) in each dataset; the membership of the modules was found to be largely concordant, and a consensus network was constructed. Further validation of the network topology showed that using approximately 35 samples is sufficient to reliably infer the transcriptome network. An in-depth analysis showed significant changes in network structure and gene connectivity associated with the selected lines; these changes were validated using a bootstrapping procedure. The most dramatic changes were associated with a gene module richly annotated with neurobehavioral traits. The changes in network connectivity were concentrated in the links between this module and the rest of the network, in addition to changes within the module; this observation is consistent with recent results in protein and metabolic networks. These results suggest that a network-based strategy will help identify the genetic factors associated with haloperidol response.</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Feb</publication><modification>2020-10-29T13:45:06Z</modification><creation>2019-03-27T01:53:08Z</creation></dates><accession>S-EPMC4460837</accession><cross_references><pubmed>21967164</pubmed><doi>10.1111/j.1601-183X.2011.00736.x</doi><doi>10.1111/j.1601-183x.2011.00736.x</doi></cross_references></HashMap>