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- Frequently Asked Questions - david. ncifcrf. gov
DAVID provides an integrated knowledgebase collected from the most common bioinformatic resources (see update of knowledgebase for details) To leverage the knowledgebase, four sets of comprehensive tools have been developed including: Functional Annotation Tools; Gene Functional Classification Tool; Gene ID Conversion Tool; Gene Name Batch Viewer
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The DAVID Knowledgebase, a backend database used for all DAVID bioinformatics tools, is built around the "DAVID Gene Concept", a single- linkage method to agglomerate tens of million of gene protein identifiers and associated annotation from dozens of well-known bio-databases
- list manager - david. ncifcrf. gov
For a single list file upload, DAVID was designed to accept the identifiers starting from the first row without a header The list needs to be in a format of one gene protein identifier per row and only the first column is considered in the analysis
- Help - david. ncifcrf. gov
It can quickly give a global idea about the gene The hyperlinks throughout the report will lead to users to original resources for further details DAVID Pathway Viewer displays user genes on static pathway maps generated by BioCarta and KEGG
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DAVID Knowledgebase gene
- DAVID usage April 2017-March 2018
DAVID API is not for high-throughput or large gene list jobs, such as a job for a gene list with more than 500 genes or trying to loop through multiple gene lists
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If you have not already registered, please do so on our registration page
- Help - david. ncifcrf. gov
With the comprehensive identifier mapping system in DAVID, many given gene protein identifiers can be quickly mapped to another based on the user's choice The tool also automatically suggests possible choices for the ambiguous gene protein identifiers in the list
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