<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Denman DJ</submitter><funding>NEI NIH HHS</funding><pagination>2707-20</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4153809</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(10)</volume><pubmed_abstract>Neural responses to sensory stimuli are not independent. Pairwise correlation can reduce coding efficiency, occur independent of stimulus representation, or serve as an additional channel of information, depending on the timescale of correlation and the method of decoding. Any role for correlation depends on its magnitude and structure. In sensory areas with maps, like the orientation map in primary visual cortex (V1), correlation is strongly related to the underlying functional architecture, but it is unclear whether this correlation structure is an essential feature of the system or arises from the arrangement of cells in the map. We assessed the relationship between functional architecture and pairwise correlation by measuring both synchrony and correlated spike count variability in mouse V1, which lacks an orientation map. We observed significant pairwise synchrony, which was organized by distance and relative orientation preference between cells. We also observed nonzero correlated variability in both the anesthetized (0.16) and awake states (0.18). Our results indicate that the structure of pairwise correlation is maintained in the absence of an underlying anatomical organization and may be an organizing principle of the mammalian visual system preserved by nonrandom connectivity within local networks.</pubmed_abstract><journal>Cerebral cortex (New York, N.Y. : 1991)</journal><pubmed_title>The structure of pairwise correlation in mouse primary visual cortex reveals functional organization in the absence of an orientation map.</pubmed_title><pmcid>PMC4153809</pmcid><funding_grant_id>P30 EY001583</funding_grant_id><funding_grant_id>R01 EY020765</funding_grant_id><funding_grant_id>2T32EY00735</funding_grant_id><funding_grant_id>T32 EY007035</funding_grant_id><pubmed_authors>Denman DJ</pubmed_authors><pubmed_authors>Contreras D</pubmed_authors></additional><is_claimable>false</is_claimable><name>The structure of pairwise correlation in mouse primary visual cortex reveals functional organization in the absence of an orientation map.</name><description>Neural responses to sensory stimuli are not independent. Pairwise correlation can reduce coding efficiency, occur independent of stimulus representation, or serve as an additional channel of information, depending on the timescale of correlation and the method of decoding. Any role for correlation depends on its magnitude and structure. In sensory areas with maps, like the orientation map in primary visual cortex (V1), correlation is strongly related to the underlying functional architecture, but it is unclear whether this correlation structure is an essential feature of the system or arises from the arrangement of cells in the map. We assessed the relationship between functional architecture and pairwise correlation by measuring both synchrony and correlated spike count variability in mouse V1, which lacks an orientation map. We observed significant pairwise synchrony, which was organized by distance and relative orientation preference between cells. We also observed nonzero correlated variability in both the anesthetized (0.16) and awake states (0.18). Our results indicate that the structure of pairwise correlation is maintained in the absence of an underlying anatomical organization and may be an organizing principle of the mammalian visual system preserved by nonrandom connectivity within local networks.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Oct</publication><modification>2025-04-19T04:18:46.625Z</modification><creation>2019-03-26T22:43:05Z</creation></dates><accession>S-EPMC4153809</accession><cross_references><pubmed>23689635</pubmed><doi>10.1093/cercor/bht128</doi></cross_references></HashMap>