{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,15]],"date-time":"2026-04-15T16:15:10Z","timestamp":1776269710257,"version":"3.50.1"},"reference-count":33,"publisher":"Oxford University Press (OUP)","issue":"10","funder":[{"name":"National Cancer Institute, National Institutes of Health","award":["HHSN261200800001E"],"award-info":[{"award-number":["HHSN261200800001E"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,10,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Motivation<\/jats:title>\n                  <jats:p>The Database for Annotation, Visualization, and Integrated Discovery (DAVID) is a web-based bioinformatics system for the functional interpretation of large lists of genes\/proteins generated from high-throughput assays. It has been cited in 72\u2009287 papers since its debut in 2003 as of 23 July 2024. The analysis is usually limited to the species of study. However, the knowledge of genes may be incomplete or unavailable for some species. Model organisms have been studied more extensively and analyzing gene lists in the context of these species can offer valuable insights, helping users better understand the genes and biological themes in their species of interest.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>We developed DAVID Ortholog for the conversion of gene lists between species. We utilized the ortholog data downloaded from Orthologous MAtrix (OMA) and Ensembl Compara as the base for the conversion. The OMA ortholog IDs and Ensembl gene IDs were converted to DAVID gene IDs and the pairing information of these IDs from these two sources was integrated into the DAVID Knowledgebase. DAVID Ortholog can convert the user\u2019s source gene list to an ortholog list of a desired species and the downstream DAVID analysis, in the context of that species, can be continued seamlessly, allowing users to further understand the biological meaning of their gene list based on the functional annotation found for the orthologs.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Availability and implementation<\/jats:title>\n                  <jats:p>https:\/\/davidbioinformatics.nih.gov\/ortholog.jsp.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1093\/bioinformatics\/btae615","type":"journal-article","created":{"date-parts":[[2024,10,16]],"date-time":"2024-10-16T14:31:44Z","timestamp":1729089104000},"source":"Crossref","is-referenced-by-count":68,"title":["DAVID Ortholog: an integrative tool to enhance functional analysis through orthologs"],"prefix":"10.1093","volume":"40","author":[{"given":"Brad T","family":"Sherman","sequence":"first","affiliation":[{"name":"Laboratory of Human Retrovirology and Immunoinformatics, Frederick National Laboratory for Cancer Research , Frederick, MD 21702,","place":["United States"]}]},{"given":"Ganesh","family":"Panzade","sequence":"additional","affiliation":[{"name":"Laboratory of Human Retrovirology and Immunoinformatics, Frederick National Laboratory for Cancer Research , Frederick, MD 21702,","place":["United States"]}]},{"given":"Tomozumi","family":"Imamichi","sequence":"additional","affiliation":[{"name":"Laboratory of Human Retrovirology and Immunoinformatics, Frederick National Laboratory for Cancer Research , Frederick, MD 21702,","place":["United States"]}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1413-2763","authenticated-orcid":false,"given":"Weizhong","family":"Chang","sequence":"additional","affiliation":[{"name":"Laboratory of Human Retrovirology and Immunoinformatics, Frederick National Laboratory for Cancer Research , 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