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ASePCR: alternative splicing electronic RT-PCR in multiple tissues and organs
Namshin Kim1, Dajeong Lim, Sanghyuk Lee
1School of Agricultural Biotechnology, Seoul National University, Seoul 151-742, Korea.
Nucleic Acids Research
|June 28, 2005
Summary
Alternative splicing (AS) generates transcript diversity, detectable via RT-PCR. ASePCR is a web tool that predicts tissue-specific transcript variants and amplicon sizes, aiding transcriptome exploration.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Alternative splicing (AS) significantly increases transcript diversity in vertebrates.
- Reverse transcription-polymerase chain reaction (RT-PCR) is a key method for detecting AS variants.
- Understanding tissue-specific gene expression is crucial for biological research.
Purpose of the Study:
- To develop an efficient web-based application, ASePCR, for predicting tissue-specific transcript variants.
- To emulate RT-PCR to estimate amplicon sizes and visualize potential isoforms in various tissues.
- To provide a resource for exploring transcriptome diversity across different species and tissues.
Main Methods:
- ASePCR utilizes NCBI's reverse e-PCR program to identify transcript models.
- It estimates amplicon sizes for user-defined primer pairs.
- Tissue specificity is determined by analyzing expressed sequence tag (EST) compatibility with transcript structures.
Main Results:
- ASePCR generates an output simulating gel electrophoresis, displaying PCR bands representing putative tissue-specific isoforms.
- The tool provides EST alignment and tissue information within a genome browser.
- Users can compare alternative splicing patterns across orthologous genes in different species.
Conclusions:
- ASePCR serves as a valuable web resource for investigating transcriptome diversity.
- It facilitates the exploration of tissue-specific alternative splicing patterns.
- The application supports multiple transcriptome models and genomes, enhancing comparative analysis.