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AsMamDB: an alternative splice database of mammals
1Institute of Bioinformatics, Tsinghua University, Beijing, 100084, China. jihk99@mails.tsinghua.edu.cn
Nucleic Acids Research
|January 11, 2000
Summary
AsMamDB is a new database for studying mammalian alternative splicing, offering data on 1563 genes from humans, mice, and rats. It provides comprehensive information on gene structures, splicing patterns, and expression, aiding genetic research.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Alternative splicing is a key mechanism for increasing proteomic diversity in mammals.
- Understanding alternative splicing is crucial for studying gene regulation and disease.
- Existing resources may not comprehensively cover mammalian alternative splicing patterns.
Purpose of the Study:
- To develop and present AsMamDB, a dedicated database for the systematic study of mammalian alternatively spliced genes.
- To provide a centralized resource for alternative splicing information in human, mouse, and rat.
- To facilitate research into gene structure, function, and expression related to alternative splicing.
Main Methods:
- Compilation of 1563 alternatively spliced genes from human, mouse, and rat.
- Integration of nucleotide sequences, gene structures, chromosomal locations, and expression data.
- Representation of alternative splicing patterns using multiple sequence alignments and topological graphs.
- Inclusion of DNA, mRNA, CDS, and EST sequences in FASTA format.
Main Results:
- AsMamDB Version 1.0 contains data for 1563 alternatively spliced genes.
- The database includes detailed information on gene structures, splicing patterns, and expression tissues.
- It links to over 130,000 GenBank entries and 4443 MEDLINE records.
- Web-based tools like Asalign are provided for data analysis.
Conclusions:
- AsMamDB serves as a valuable resource for researchers studying mammalian alternative splicing.
- The database facilitates systematic investigation of gene regulation and proteomic diversity.
- It supports comparative genomics and functional studies of alternatively spliced genes.