<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang S</submitter><funding>U.S. Department of Health and Human Services</funding><funding>NIAID NIH HHS</funding><funding>School of Dental Medicine, University of Pittsburgh</funding><funding>National Institutes of Health</funding><funding>NIAID</funding><pagination>1278-1294.e4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11659032</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(12)</volume><pubmed_abstract>Analysis of multi-modal datasets can identify multi-scale interactions underlying biological systems but can be beset by spurious connections due to indirect impacts propagating through an unmapped biological network. For example, studies in macaques have shown that Bacillus Calmette-Guerin (BCG) vaccination by an intravenous route protects against tuberculosis, correlating with changes across various immune data modes. To eliminate spurious correlations and identify critical immune interactions in a public multi-modal dataset (systems serology, cytokines, and cytometry) of vaccinated macaques, we applied Markov fields (MFs), a data-driven approach that explains vaccine efficacy and immune correlations via multivariate network paths, without requiring large numbers of samples (i.e., macaqu</pubmed_abstract><journal>Cell systems</journal><pubmed_title>Markov field network model of multi-modal data predicts effects of immune system perturbations on intravenous BCG vaccination in macaques.</pubmed_title><pmcid>PMC11659032</pmcid><funding_grant_id>75N93019C00071</funding_grant_id><funding_grant_id>F31 AI150171</funding_grant_id><funding_grant_id>AI150171</funding_grant_id><funding_grant_id>U19 AI167899</funding_grant_id><funding_grant_id>AI167899</funding_grant_id><pubmed_authors>Chao MC</pubmed_authors><pubmed_authors>Kracinovsky K</pubmed_authors><pubmed_authors>Lin PL</pubmed_authors><pubmed_authors>Flynn JL</pubmed_authors><pubmed_authors>Lauffenburger DA</pubmed_authors><pubmed_authors>Roederer M</pubmed_authors><pubmed_authors>Fortune SM</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Tomko J</pubmed_authors><pubmed_authors>Scanga CA</pubmed_authors><pubmed_authors>Myers AJ</pubmed_authors><pubmed_authors>Seder RA</pubmed_authors><pubmed_authors>Alter G</pubmed_authors><pubmed_authors>Rodgers MA</pubmed_authors><pubmed_authors>Mugahid D</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Borish HJ</pubmed_authors><pubmed_authors>Irvine EB</pubmed_authors><pubmed_authors>Darrah PA</pubmed_authors><pubmed_authors>Maiello P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Markov field network model of multi-modal data predicts effects of immune system perturbations on intravenous BCG vaccination in macaques.</name><description>Analysis of multi-modal datasets can identify multi-scale interactions underlying biological systems but can be beset by spurious connections due to indirect impacts propagating through an unmapped biological network. For example, studies in macaques have shown that Bacillus Calmette-Guerin (BCG) vaccination by an intravenous route protects against tuberculosis, correlating with changes across various immune data modes. To eliminate spurious correlations and identify critical immune interactions in a public multi-modal dataset (systems serology, cytokines, and cytometry) of vaccinated macaques, we applied Markov fields (MFs), a data-driven approach that explains vaccine efficacy and immune correlations via multivariate network paths, without requiring large numbers of samples (i.e., macaqu</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-06-06T04:12:42.265Z</modification><creation>2026-05-25T03:12:01.112Z</creation></dates><accession>S-EPMC11659032</accession><cross_references><pubmed>39504969</pubmed><doi>10.1016/j.cels.2024.10.001</doi></cross_references></HashMap>