DNannotator
DNannotator performs de novo annotation and integration of genomic features, including single nucleotide polymorphisms (SNPs), sequence-tagged sites (STSs), and exons, to support genomic data mining and high-throughput experiment design.
Key Features:
- De novo annotation: Performs de novo annotation of genomic regions targeting SNPs, STSs, and exons.
- Batch annotation: Accepts annotation source data such as SNPs, genes, primers, and specified genomic targets for batch processing of large datasets.
- Annotation migration: Migrates existing annotations in GenBank format from one sequence to another to accommodate sequence updates and different sequence versions for sequences less than 30 kilobases.
- Output formats: Produces results in GenBank format and tab-delimited text files for importation into databases or spreadsheets.
- Visualization compatibility: Generates outputs compatible with graphic viewers such as the Genome Browser and Artemis.
- Quality evaluation: Optionally provides reference data reports to evaluate the quality of annotations.
Scientific Applications:
- Gene and marker discovery: Support development of local discoveries such as genes and genetic markers from annotated genomic regions.
- Annotation integration: Facilitate collection and integration of annotations from multiple resources into a unified dataset.
- High-throughput experimental design: Enable design of high-throughput experiments based on integrated annotated genomic data.
Methodology:
Accepts user-defined or specified target data, performs de novo annotation of SNPs, STSs, and exons, and migrates existing GenBank annotations between sequences.
Topics
Details
- Tool Type:
- web application
- Added:
- 2/10/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Liu C. DNannotator: annotation software tool kit for regional genomic sequences. Nucleic Acids Research. 2003;31(13):3729-3735. doi:10.1093/nar/gkg542. PMID:12824405. PMCID:PMC168949.
Nguyen TH, Liu C, Gershon ES, McMahon FJ. Frequency Finder: a multi-source web application for collection of public allele frequencies of SNP markers. Bioinformatics. 2004;20(3):439-443. doi:10.1093/bioinformatics/btg446. PMID:14960477.