Suchergebnisse
Suchergebnisse:
17. Apr. 2024 · DAVID is a database and a set of tools for analyzing gene lists and finding biological themes, pathways, and interactions. It is used by researchers from over 100 countries and has over 69K citations.
- Functional Annotation Functional Annotation Clustering Functional Annotation Chart Functional Annotation Table
Functional Annotation Functional Annotation Clustering...
- Gene Functional Classification
Gene Functional Classification - DAVID Functional Annotation...
- Gene ID Conversion
Gene ID Conversion - DAVID Functional Annotation...
- Gene Name Batch Viewer
Gene Name Batch Viewer - DAVID Functional Annotation...
- Tutorial
The Functional Annotation Summary provides annotation type...
- FAQ
FAQ - DAVID Functional Annotation Bioinformatics Microarray...
- LHRI Publications
LHRI Publications - DAVID Functional Annotation...
- LHRI Presentations
LHRI Presentations - DAVID Functional Annotation...
- Functional Annotation Functional Annotation Clustering Functional Annotation Chart Functional Annotation Table
20. Jan. 2021 · Fisher's Exact p -values are computed by summing probabilities p over defined sets of tables (Prob=∑ Ap ). For 2 x 2 tables, one-sided p -values for Fisher's Exact test are defined in terms of the frequency of the cell in the first rows and first column of the table, the (1,1) cell. Denote the observed (1,1) cell frequency by n11, for a right ...
23. März 2022 · DAVID is a popular bioinformatics resource system including a web server and web service for functional annotation and enrichment analyses of gene lists. It consists of a comprehensive knowledgebase and a set of functional analysis tools. Here, we report all updates made in 2021.
14. Juli 2020 · This tutorial shows you how to generate a variety of functional annotations of a gene list, such as that generated by differential gene expression analyses l...
- 13 Min.
- 69,4K
- Genomics Guru
14. Aug. 2003 · DAVID, a web-accessible program that integrates functional genomic annotations with intuitive graphical summaries, has been described and will assist in the interpretation of genome-scale datasets by facilitating the transition from data collection to biological meaning.
README. For given genes, to access the corresponding heterogeneous functional annotations, which cover over 50 categories from dozens of public databases , in a high-throughput manner. For given gene identifiers, to translate to other types of gene identifiers representing the same gene entries in a high-throughput manner.
