1 / 7

Biological Information Integration Toolkit

Biological Information Integration Toolkit. Jeremy Praissman, Dawei Lin, John Rose, Bi-Cheng Wang. Motivation. Calculate simple properties of genomes and group genes according to these properties Tie together and integrate data and analyses (Blast results, annotation etc.).

fleur-solis
Download Presentation

Biological Information Integration Toolkit

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Biological Information Integration Toolkit Jeremy Praissman, Dawei Lin, John Rose, Bi-Cheng Wang

  2. Motivation • Calculate simple properties of genomes and group genes according to these properties • Tie together and integrate data and analyses (Blast results, annotation etc.) Accomplish the above in a way that provides additional support for implementing new bioinformatics algorithms

  3. Genomes & Genes Genome Data Structure • Loads data and initializes other data structures • Exports most of the functionality of the Strand data structure (described below) • Contains “Gene” objects which are wrappers for BioPython SeqFeatures Gene Data Structure • Calculate upstream/downstream intergenic distance (IGD) • Easily generate subsequences relative to gene location

  4. Strands • A list of Genes - represents a strand of biological information • Implicit intergenic regions Functionality • Base object for computing statistics • Number of sequence features (total, overlapping etc..) • Number of bases (in overlapping areas of features, in features etc..) • Generate new Strands based on IGD • Filter and map operations for obtaining “Sets”

  5. Sets • Unordered collection of objects • Supports: • Membership testing • Union • Intersection • Other set operations Example: set_1 = all Genes in a Genome with start codon GTG set_2 = all Genes in a Genome with upstream igd < 20 set_3 = set_1.intersect(set_2) is the set containing all Genes in the Genome with both properties

  6. Graphs • Combinatorial graph data structures and algorithms • Vertices tied to Genes, edges represent relationships between Genes Functionality • Support for linking vertices based on gene properties • Additional support class (Similarity) for building graphs using blast data and user supplied parameters • Tarjan’s fast (O(v + e)) algorithm for finding strongly connected components • Johnson’s fast (O(v + e) * c) algorithm for finding elementary circuits

  7. Acknowledgements • Dr. Dawei Lin • Dr. John Rose • Dr. B.C. Wang • The BioPython people • The BioPerl people http://www.secsg.org

More Related