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Related Experiment Videos

SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant

Ari B Kahn1, Michael C Ryan, Hongfang Liu

  • 1Department of Bioinformatics, George Mason University, Fairfax, Virginia, USA. arik@mail.nih.gov <arik@mail.nih.gov>

BMC Bioinformatics
|March 7, 2007
PubMed
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Alternative splicing generates diverse human transcripts from limited genes. SpliceMiner, a web tool querying the Evidence Viewer Database (EVDB), enables high-throughput analysis of splice variants, improving microarray data interpretation.

Area of Science:

  • Bioinformatics
  • Genomics
  • Molecular Biology

Background:

  • The human genome contains fewer genes than expressed transcripts, primarily due to alternative splicing.
  • Alternative splicing produces tissue-specific, developmental stage-specific, and condition-specific transcripts.
  • Accurate analysis of microarray data and new array design for alternative splicing necessitate probe-level sequence and exon assessment.

Purpose of the Study:

  • To develop SpliceMiner, a web interface for querying the Evidence Viewer Database (EVDB).
  • To provide a comprehensive, non-redundant compendium of human splice variant data.
  • To enable high-throughput batch queries and facilitate probe-to-splice variant mapping.

Main Methods:

  • Constructed EVDB as a queryable implementation of the NCBI Evidence Viewer (EV).

Related Experiment Videos

  • Utilized data from NCBI Entrez Gene and EV, filtering for complete coding sequences and non-redundant splice variants.
  • Developed SpliceMiner as a user-friendly web interface for querying EVDB by gene symbol, genomic coordinates, or probe sequence.
  • Main Results:

    • EVDB provides a comprehensive compendium of human splice variant data.
    • SpliceMiner supports high-throughput batch queries, unlike the single-query EV.
    • SpliceMiner effectively maps probes to specific splice variants.

    Conclusions:

    • The EVDB/SpliceMiner combination offers a powerful interface for human splice variant information.
    • This tool facilitates fluent, high-throughput analysis, enhancing the NCBI Evidence Viewer.
    • Integrating EVDB/SpliceMiner into microarray pipelines can improve gene expression data analysis and bioinformatic interpretation, aiding in the identification of splice variant issues.