Literature DB >> 12050073

Gene structure identification with MyGV using cDNA evidence and protein homologs to improve ab initio predictions.

Wei Zhu1, Volker Brendel.   

Abstract

UNLABELLED: MyGV is an application to visualize (potentially genome-scale) gene structure annotation and prediction. The output of any external gene prediction program can be easily converted to a generalized format for input into MyGV. The application displays all input simultaneously in graphical representation, with a toggle option for a text-based view. Zooming capabilities allow detailed comparisons for specific genome locations. The tool is particularly helpful for refinement of ab initio predicted gene structures by spliced alignment with cDNA or protein homologs. AVAILABILITY: The program was written in Java and is freely available to non-commercial users by electronic download from http://bioinformatics.iastate.edu/bioinformatics2go/MyGV.

Mesh:

Year:  2002        PMID: 12050073     DOI: 10.1093/bioinformatics/18.5.761

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  4 in total

1.  The maize genome contains a helitron insertion.

Authors:  Shailesh K Lal; Michael J Giroux; Volker Brendel; C Eduardo Vallejos; L Curtis Hannah
Journal:  Plant Cell       Date:  2003-02       Impact factor: 11.277

2.  GeneSeqer@PlantGDB: Gene structure prediction in plant genomes.

Authors:  Shannon D Schlueter; Qunfeng Dong; Volker Brendel
Journal:  Nucleic Acids Res       Date:  2003-07-01       Impact factor: 16.971

3.  A novel class of Helitron-related transposable elements in maize contain portions of multiple pseudogenes.

Authors:  Smriti Gupta; Andrea Gallavotti; Gabrielle A Stryker; Robert J Schmidt; Shailesh K Lal
Journal:  Plant Mol Biol       Date:  2005-01       Impact factor: 4.076

4.  Gene discovery and transcript analyses in the corn smut pathogen Ustilago maydis: expressed sequence tag and genome sequence comparison.

Authors:  Eric C H Ho; Matt J Cahill; Barry J Saville
Journal:  BMC Genomics       Date:  2007-09-24       Impact factor: 3.969

  4 in total

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