Alternative splicing and functional prediction analysis tool
AltAnalyze - From AltAnalyze's main window you will be able to select the database version and the species you want to analyze.
  5 Screenshots
AltAnalyze is an open source and cross-platform utility that will allow you to take RNASeq or relatively raw microarray data (CEL files or normalized), identify predicted alternative splicing or alternative promoter changes and view how these changes may affect protein sequence, domain composition, and microRNA targeting.

AltAnalyze is compatible with any RNASeq data (exons and/or junctions), several Affymetrix splicing sensitive array types (Gene 1.0, Exon 1.0, junction) as well as many conventional array-types (e.g., Illumina, Agilent, Affymetrix).

AltAnalyze can be used either as a command-line or as a graphical user interface based app, and it requires no advanced knowledge of bioinformatics programs or scripting.

Alternative regulated exons can be subsequently visualized in the context of proteins, domains and microRNA binding sites with the Cytoscape Plugin DomainGraph.

last updated on:
January 22nd, 2014, 7:58 GMT
file size:
111.9 MB
license type:
developed by:
Nathan Salomonis and Bruce Conklin
operating system(s):
Mac OS X
binary format:
Universal Binary
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5 Screenshots
AltAnalyze - The Download File Status window displays the status information related to the downloaded files and databases.AltAnalyze - From AltAnalyze's Main Dataset Parameters you can select the vendor or data type, the species and platform.AltAnalyzeAltAnalyze
What's New in This Release:
  • Numerous bug fixes (listed in FeaturesToImplement),
  • Multiple new accessory tools added: interactive network analysis and visualization, 3D PCA, identifier translator, alternative exon viewer, Venn Diagram viewer, and file merger,
  • MarkerFinder algorithm included to unique find marker genes for each condition,
  • Customizable hierarchical clustering visualization options and associated ontology/gene-set/gene correlation/filtering options ,
read full changelog

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