<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang H</submitter><funding>NICHD NIH HHS</funding><funding>NIH/NICHD</funding><pagination>14</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8740472</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Interferon regulatory factor-8 (IRF8) and nuclear factor-activated T cells c1 (NFATc1) are two transcription factors that have an important role in osteoclast differentiation. Thanks to ChIP-seq technology, scientists can now estimate potential genome-wide target genes of IRF8 and NFATc1. However, finding target genes that are consistently up-regulated or down-regulated across different studies is hard because it requires analysis of a large number of high-throughput expression studies from a comparable context.&lt;h4>Method&lt;/h4>We have developed a machine learning based method, called, Cohort-based TF target prediction system (cTAP) to overcome this problem. This method assumes that the pathway involving the transcription factors of interest is featured with multiple "func</pubmed_abstract><journal>BMC genomics</journal><pubmed_title>Predicting the targets of IRF8 and NFATc1 during osteoclast differentiation using the machine learning method framework cTAP.</pubmed_title><pmcid>PMC8740472</pmcid><funding_grant_id>R01 HD098636</funding_grant_id><funding_grant_id>1R01HD098636-0</funding_grant_id><pubmed_authors>Joshi P</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Maye PF</pubmed_authors><pubmed_authors>Rowe DW</pubmed_authors><pubmed_authors>Hong SH</pubmed_authors><pubmed_authors>Shin DG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Predicting the targets of IRF8 and NFATc1 during osteoclast differentiation using the machine learning method framework cTAP.</name><description>&lt;h4>Background&lt;/h4>Interferon regulatory factor-8 (IRF8) and nuclear factor-activated T cells c1 (NFATc1) are two transcription factors that have an important role in osteoclast differentiation. Thanks to ChIP-seq technology, scientists can now estimate potential genome-wide target genes of IRF8 and NFATc1. However, finding target genes that are consistently up-regulated or down-regulated across different studies is hard because it requires analysis of a large number of high-throughput expression studies from a comparable context.&lt;h4>Method&lt;/h4>We have developed a machine learning based method, called, Cohort-based TF target prediction system (cTAP) to overcome this problem. This method assumes that the pathway involving the transcription factors of interest is featured with multiple "func</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-21T17:38:42.58Z</modification><creation>2022-02-11T15:09:04.606Z</creation></dates><accession>S-EPMC8740472</accession><cross_references><pubmed>34991467</pubmed><doi>10.1186/s12864-021-08159-z</doi></cross_references></HashMap>