Exact(1)
To examine the potential biological impact of these transcriptome alterations we undertook Gene Ontology (GO) analysis using the DAVID suite to identify significantly over-expressed biological pathways within the subset of transcripts regulated by PCN-alone, LCA-alone or by both chemicals.
Similar(59)
Total for each subpopulation is a sum of deletions and duplications in each subpopulation The genes affected by CNVRs in all Qataris were evaluated by standard pathway analysis against the KEGG pathway database using the DAVID bioinformatics suite [ 31– 31].
A gene ontology (GO) analysis was performed using the DAVID website.
Using the DAVID functional annotation clustering tool, the up- and down-regulated genes can be categorized into 176 and 146 overlapping functional gene clusters, respectively.
Differentially expressed genes were categorized in GeneOntology groups using the DAVID tool (http://david.abcc.ncifcrf.gov/).abcc.ncifcrf.gov/
Functional clustering was performed using the DAVID database.
We analyzed the 1,817 genes that were hypermethylated only in RL cells using the DAVID interface (http://david.abcc.ncifcrf.gov/).abcc.ncifcrf.gov/
Functional annotation and enrichment analyses were done using the DAVID platform version 6.7 (http://david.abcc.ncifcrf.gov/home.jsp) [36], [37].
The Gene Ontology (GO) terms and KEGG pathways of targeted genes were annotated using the DAVID gene annotation tool (http://david.abcc.ncifcrf.gov/UTH).abcc.ncifcrf.gov/UTH
KEGG pathway enrichment analysis was performed using the DAVID web server (http://david.abcc.ncifcrf.gov/home.jsp).jsp
Functional classification of differentially expressed proteins was performed using the DAVID software (http://david.abcc.ncifcrf.gov/).abcc.ncifcrf.gov/
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