SeqFreed
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SeqFreed is a bioinformatics desktop. It provides efficient and user-friendly access to sequence data and gene features. Its customizable command line interface runs locally installed bioinformatic tools in a convenient way. Seqfreeds flexible display of either text or images in different page modes enhances ease and productivity of routine molecular biology analysis. SeqFreed is written in Python using GTK+ and runs on Linux.

SeqFreed 0.01 released - 02 Apr 2006

Welcome.
This is the first release of SeqFreed, a bioinformatics desktop.
The basic design of SeqFreeds webpage was copied from the Comix site (comix.sourceforge.net) with the permission of Pontus Ekberg. Thank you, Pontus!
screenshot SeqFreed in dual page mode.

Features

  • -- Sequence and feature extraction from multiple GenBank files.
  • -- Database like access to sequence data:
    • Protein or DNA.
    • Full length sequences or subsequences.
    • Coding or noncoding regions.
    • Sequence access by gene name, locus tag or absolute coordinates.
  • -- Fast, index-driven lookup.
  • -- Batch lookup: arbitray number of gene queries processed at once.
  • -- Customizable command line (history) with entry completion.
  • -- Page content is piped as input to the invoked application.
  • -- Results are directly read from stdin and displayed as either text or image.
  • -- Single page, double page and "full screen" mode.
  • -- 20 notebook pages for text or image display.
  • -- Text font size scalable.
  • -- Image size scalable.
  • -- Convenient "single-click-copy" and "single-click-append".
  • -- Page lock prevents accidental overwrite.
  • -- Images saved as PNG.
  • -- User definable auxiliary pages.
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